CA1066840A - Resines de type n-cyanosulfonamide, composes intermediaires voisins et produits a base de ceux-ci - Google Patents

Resines de type n-cyanosulfonamide, composes intermediaires voisins et produits a base de ceux-ci

Info

Publication number: CA1066840A
Authority: CA; Canada
Prior art keywords: bis; cyanamide; polymer; mole; cyanosulfonamide
Prior art date: 1974-02-04
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA313,331A

Other languages

English (en)

Inventor

Raymond J. Kray

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novartis AG

Original Assignee

Ciba Geigy AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1974-02-04

Filing date

1978-10-13

Publication date

1979-11-20

1974-02-04 Priority claimed from US05/439,487 external-priority patent/US3944526A/en

1978-10-13 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1978-10-13 Priority to CA313,331A priority Critical patent/CA1066840A/fr

1979-11-20 Application granted granted Critical

1979-11-20 Publication of CA1066840A publication Critical patent/CA1066840A/fr

Status Expired legal-status Critical Current

Links

229920005989 resin Polymers 0.000 title abstract description 39
239000011347 resin Substances 0.000 title abstract description 39
LDABEQINUALFMV-UHFFFAOYSA-N O=S(=O)NC#N Chemical compound O=S(=O)NC#N LDABEQINUALFMV-UHFFFAOYSA-N 0.000 title description 5
239000000543 intermediate Substances 0.000 title 1
238000012644 addition polymerization Methods 0.000 claims abstract description 6
239000011248 coating agent Substances 0.000 claims abstract description 4
238000000576 coating method Methods 0.000 claims abstract description 4
-1 N-cyanosulfonamide compound Chemical class 0.000 claims description 30
XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 26
229920000642 polymer Polymers 0.000 claims description 25
125000003118 aryl group Chemical group 0.000 claims description 16
125000001931 aliphatic group Chemical group 0.000 claims description 14
239000011521 glass Substances 0.000 claims description 9
238000006116 polymerization reaction Methods 0.000 claims description 9
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 5
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
229910052796 boron Inorganic materials 0.000 claims description 3
238000007334 copolymerization reaction Methods 0.000 claims description 3
235000013350 formula milk Nutrition 0.000 claims 10
239000000758 substrate Substances 0.000 claims 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
241000534944 Thia Species 0.000 claims 2
125000002947 alkylene group Chemical group 0.000 claims 2
125000001118 alkylidene group Chemical group 0.000 claims 2
125000003368 amide group Chemical group 0.000 claims 2
239000004760 aramid Substances 0.000 claims 2
229920003235 aromatic polyamide Polymers 0.000 claims 2
125000004467 aryl imino group Chemical group 0.000 claims 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
QWJNFFYFEKXZBF-UHFFFAOYSA-N cyanocyanamide Chemical compound N#CNC#N QWJNFFYFEKXZBF-UHFFFAOYSA-N 0.000 claims 2
229910002804 graphite Inorganic materials 0.000 claims 2
239000010439 graphite Substances 0.000 claims 2
125000004957 naphthylene group Chemical group 0.000 claims 2
239000000203 mixture Substances 0.000 abstract description 16
238000000465 moulding Methods 0.000 abstract description 10
238000010030 laminating Methods 0.000 abstract description 6
238000005266 casting Methods 0.000 abstract description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 39
239000000243 solution Substances 0.000 description 36
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 19
150000001875 compounds Chemical class 0.000 description 19
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 18
150000002500 ions Chemical class 0.000 description 18
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
239000002904 solvent Substances 0.000 description 14
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
238000010438 heat treatment Methods 0.000 description 11
238000000034 method Methods 0.000 description 11
239000000843 powder Substances 0.000 description 10
239000010408 film Substances 0.000 description 9
JLXXLCJERIYMQG-UHFFFAOYSA-N phenylcyanamide Chemical compound N#CNC1=CC=CC=C1 JLXXLCJERIYMQG-UHFFFAOYSA-N 0.000 description 9
239000007787 solid Substances 0.000 description 9
239000002966 varnish Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
238000004458 analytical method Methods 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
125000004093 cyano group Chemical group *C#N 0.000 description 8
JMANVNJQNLATNU-UHFFFAOYSA-N glycolonitrile Natural products N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000004744 fabric Substances 0.000 description 7
230000009477 glass transition Effects 0.000 description 7
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
238000009835 boiling Methods 0.000 description 6
150000003949 imides Chemical class 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
239000000047 product Substances 0.000 description 6
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 6
230000032683 aging Effects 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
230000000717 retained effect Effects 0.000 description 5
HJEINPVZRDJRBY-UHFFFAOYSA-N Disul Chemical compound OS(=O)(=O)OCCOC1=CC=C(Cl)C=C1Cl HJEINPVZRDJRBY-UHFFFAOYSA-N 0.000 description 4
239000004952 Polyamide Substances 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
238000001035 drying Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 4
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230000008569 process Effects 0.000 description 4
229920001187 thermosetting polymer Polymers 0.000 description 4
230000007704 transition Effects 0.000 description 4
125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 3
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 3
LQVXSNNAFNGRAH-QHCPKHFHSA-N BMS-754807 Chemical compound C([C@@]1(C)C(=O)NC=2C=NC(F)=CC=2)CCN1C(=NN1C=CC=C11)N=C1NC(=NN1)C=C1C1CC1 LQVXSNNAFNGRAH-QHCPKHFHSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
230000006835 compression Effects 0.000 description 3
238000007906 compression Methods 0.000 description 3
150000001912 cyanamides Chemical class 0.000 description 3
QPJDMGCKMHUXFD-UHFFFAOYSA-N cyanogen chloride Chemical compound ClC#N QPJDMGCKMHUXFD-UHFFFAOYSA-N 0.000 description 3
150000004820 halides Chemical class 0.000 description 3
238000005259 measurement Methods 0.000 description 3
239000000155 melt Substances 0.000 description 3
VBOBDSYQEZUOGV-UHFFFAOYSA-N n-cyano-n-phenylbenzenesulfonamide Chemical compound C=1C=CC=CC=1S(=O)(=O)N(C#N)C1=CC=CC=C1 VBOBDSYQEZUOGV-UHFFFAOYSA-N 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
229940124530 sulfonamide Drugs 0.000 description 3
150000003456 sulfonamides Chemical class 0.000 description 3
239000000725 suspension Substances 0.000 description 3
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical group C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 2
USQCUKQZXOWUDF-YWZLYKJASA-N 6-chloro-n-[(3s)-1-[(2s)-1-(4-methyl-5-oxo-1,4-diazepan-1-yl)-1-oxopropan-2-yl]-2-oxopyrrolidin-3-yl]naphthalene-2-sulfonamide Chemical compound O=C([C@@H](N1C([C@@H](NS(=O)(=O)C=2C=C3C=CC(Cl)=CC3=CC=2)CC1)=O)C)N1CCN(C)C(=O)CC1 USQCUKQZXOWUDF-YWZLYKJASA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
OPFTUNCRGUEPRZ-QLFBSQMISA-N Cyclohexane Natural products CC(=C)[C@@H]1CC[C@@](C)(C=C)[C@H](C(C)=C)C1 OPFTUNCRGUEPRZ-QLFBSQMISA-N 0.000 description 2
RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
102000006835 Lamins Human genes 0.000 description 2
108010047294 Lamins Proteins 0.000 description 2
SAXCJMNOBJEGSR-UHFFFAOYSA-N N#CNC(C=CC=C1)C1=S(=O)=O Chemical compound N#CNC(C=CC=C1)C1=S(=O)=O SAXCJMNOBJEGSR-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
HFDDMEQYUSCTJR-UHFFFAOYSA-N NC#N.NC#N.O=S(=O)NC#N Chemical compound NC#N.NC#N.O=S(=O)NC#N HFDDMEQYUSCTJR-UHFFFAOYSA-N 0.000 description 2
241001387976 Pera Species 0.000 description 2
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CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 2
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229910052736 halogen Inorganic materials 0.000 description 2
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ATADHKWKHYVBTJ-UHFFFAOYSA-N hydron;4-[1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol;chloride Chemical compound Cl.CNCC(O)C1=CC=C(O)C(O)=C1 ATADHKWKHYVBTJ-UHFFFAOYSA-N 0.000 description 2
QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
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NIQQIJXGUZVEBB-UHFFFAOYSA-N methanol;propan-2-one Chemical compound OC.CC(C)=O NIQQIJXGUZVEBB-UHFFFAOYSA-N 0.000 description 2
239000000178 monomer Substances 0.000 description 2
APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 2
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
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238000007654 immersion Methods 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
DKZQZHQHDMVGHE-UHFFFAOYSA-N methanedisulfonyl chloride Chemical compound ClS(=O)(=O)CS(Cl)(=O)=O DKZQZHQHDMVGHE-UHFFFAOYSA-N 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
FJKUZZHKEDNPDN-UHFFFAOYSA-N naphthalene-2,7-disulfonyl chloride Chemical compound C1=CC(S(Cl)(=O)=O)=CC2=CC(S(=O)(=O)Cl)=CC=C21 FJKUZZHKEDNPDN-UHFFFAOYSA-N 0.000 description 1
OPECTNGATDYLSS-UHFFFAOYSA-N naphthalene-2-sulfonyl chloride Chemical compound C1=CC=CC2=CC(S(=O)(=O)Cl)=CC=C21 OPECTNGATDYLSS-UHFFFAOYSA-N 0.000 description 1
HYWYRSMBCFDLJT-UHFFFAOYSA-N nimesulide Chemical compound CS(=O)(=O)NC1=CC=C([N+]([O-])=O)C=C1OC1=CC=CC=C1 HYWYRSMBCFDLJT-UHFFFAOYSA-N 0.000 description 1
229960000965 nimesulide Drugs 0.000 description 1
125000002560 nitrile group Chemical group 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
WIVNTNLDTMNDNO-UHFFFAOYSA-N octane-1-sulfonyl chloride Chemical class CCCCCCCCS(Cl)(=O)=O WIVNTNLDTMNDNO-UHFFFAOYSA-N 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
238000002103 osmometry Methods 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
PWQOZRPSDQKNPW-UHFFFAOYSA-N pentane-1-sulfonyl chloride Chemical compound CCCCCS(Cl)(=O)=O PWQOZRPSDQKNPW-UHFFFAOYSA-N 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000012704 polymeric precursor Substances 0.000 description 1
238000004382 potting Methods 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000002243 precursor Substances 0.000 description 1
230000002028 premature Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
KPBSJEBFALFJTO-UHFFFAOYSA-N propane-1-sulfonyl chloride Chemical compound CCCS(Cl)(=O)=O KPBSJEBFALFJTO-UHFFFAOYSA-N 0.000 description 1
DRINJBFRTLBHNF-UHFFFAOYSA-N propane-2-sulfonyl chloride Chemical compound CC(C)S(Cl)(=O)=O DRINJBFRTLBHNF-UHFFFAOYSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000002076 thermal analysis method Methods 0.000 description 1
238000002411 thermogravimetry Methods 0.000 description 1
239000004634 thermosetting polymer Substances 0.000 description 1
239000010409 thin film Substances 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
238000001721 transfer moulding Methods 0.000 description 1
GRGCWBWNLSTIEN-UHFFFAOYSA-N trifluoromethanesulfonyl chloride Chemical compound FC(F)(F)S(Cl)(=O)=O GRGCWBWNLSTIEN-UHFFFAOYSA-N 0.000 description 1
239000002759 woven fabric Substances 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)

CA313,331A 1974-02-04 1978-10-13 Resines de type n-cyanosulfonamide, composes intermediaires voisins et produits a base de ceux-ci Expired CA1066840A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA313,331A CA1066840A (fr)	1974-02-04	1978-10-13	Resines de type n-cyanosulfonamide, composes intermediaires voisins et produits a base de ceux-ci

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US05/439,487 US3944526A (en)	1974-02-04	1974-02-04	N-cyanosulfonamide resins and intermediates therefor and products thereof
CA218,803A CA1066719A (fr)	1974-02-04	1975-01-28	Resines de n-cyanosulfonamide, composes intermediaires et produits
CA313,331A CA1066840A (fr)	1974-02-04	1978-10-13	Resines de type n-cyanosulfonamide, composes intermediaires voisins et produits a base de ceux-ci

Publications (1)

Publication Number	Publication Date
CA1066840A true CA1066840A (fr)	1979-11-20

Family

ID=27163797

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA313,331A Expired CA1066840A (fr)	1974-02-04	1978-10-13	Resines de type n-cyanosulfonamide, composes intermediaires voisins et produits a base de ceux-ci

Country Status (1)

Country	Link
CA (1)	CA1066840A (fr)

1978
- 1978-10-13 CA CA313,331A patent/CA1066840A/fr not_active Expired

Publication	Publication Date	Title
US5243023A (en)	1993-09-07	Polyimides containing amide and perfluoroisopropylidene connecting groups
CA1076294A (fr)	1980-04-22	Polyamides-imides solubles, derives de diamines de phenylindane
US5145937A (en)	1992-09-08	Polyimides with carbonyl and ether connecting groups between the aromatic rings
US4600769A (en)	1986-07-15	Amine terminated bisaspartimide polymer
US4876325A (en)	1989-10-24	Polyimide resin from bis-imide, polyphenol and dicyandiamide
US4238591A (en)	1980-12-09	Novel copolymers of imido monomer/hydroxylated organosilicon comonomer
US4820791A (en)	1989-04-11	Polyimides containing carbonyl and ether connecting groups
US4075185A (en)	1978-02-21	N-cyanosulfonamide resins and intermediates therefor and products thereof
CA1061929A (fr)	1979-09-04	Polymeres traitables a haute temperature
US4959443A (en)	1990-09-25	Thermosetting resin composition from bis maleimide and aromatic amine resin
CA1066719A (fr)	1979-11-20	Resines de n-cyanosulfonamide, composes intermediaires et produits
US4361690A (en)	1982-11-30	Novel imido/hydroxylate organosilicon copolymers
US4049711A (en)	1977-09-20	N-cyanosulfonamides
CA1139494A (fr)	1983-01-11	Polyimides de bismaleimides et composes actives a base de methylene
CA1335856C (fr)	1995-06-06	Materiaux de moulage thermodurcissables a base de dimaleimide
DE2513731A1 (de)	1975-10-09	Verfahren zur herstellung von polymeren, die s-triazinringe enthalten
CA2028364C (fr)	1995-02-14	Compositions de resine thermodurcissable
US4962161A (en)	1990-10-09	Thermosettable resin compositions
US4150051A (en)	1979-04-17	N-Cyanosulfonamide compounds
CA2028312C (fr)	1996-03-12	Composition formant une resine thermodurcissable et procede pour sa preparation
US3814719A (en)	1974-06-04	Zeta-triazine-imide copolymers
US5095074A (en)	1992-03-10	Thermosettable resin compositions
US5206383A (en)	1993-04-27	o,o'-bismaleimide resin systems
Takahashi et al.	1991	Thermal behavior and reactivities of prepolymers prepared from aromatic biscyanamides and bismaleimide
CA1304535C (fr)	1992-06-30	Derives insatures d'imides et de benzaldehyde renfermant des compositions thermodurcissables