JPS5962552A - ｐ−ニトロソ−フエノ−ルのアミン塩及びその製造方法 - Google Patents

ｐ−ニトロソ−フエノ−ルのアミン塩及びその製造方法

Info

Publication number: JPS5962552A
Authority: JP; Japan
Prior art keywords: salt; nitroso; phenol; carbon atoms; group
Prior art date: 1982-08-04
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.): Pending

Application number

JP58141974A

Other languages

English (en)

Japanese (ja)

Inventor

イソム・イ−・ワゴナ−

ル−ス・ハドソン

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.)

Sandoz AG

Original Assignee

Sandoz 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.)

1982-08-04

Filing date

1983-08-04

Publication date

1984-04-10

1983-08-04 Application filed by Sandoz AG filed Critical Sandoz AG

1984-04-10 Publication of JPS5962552A publication Critical patent/JPS5962552A/ja

Status Pending legal-status Critical Current

Links

JSTCPNFNKICNNO-UHFFFAOYSA-N 4-nitrosophenol Chemical class OC1=CC=C(N=O)C=C1 JSTCPNFNKICNNO-UHFFFAOYSA-N 0.000 title claims description 50
-1 Amine salts Chemical class 0.000 title claims description 32
238000004519 manufacturing process Methods 0.000 title claims description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 38
150000001875 compounds Chemical class 0.000 claims description 34
150000003839 salts Chemical class 0.000 claims description 33
229920000768 polyamine Chemical class 0.000 claims description 25
125000000217 alkyl group Chemical group 0.000 claims description 22
239000000178 monomer Substances 0.000 claims description 21
150000001412 amines Chemical group 0.000 claims description 20
238000006116 polymerization reaction Methods 0.000 claims description 18
239000000203 mixture Chemical group 0.000 claims description 13
125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 10
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 claims description 9
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical group C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims description 6
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 6
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 5
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 5
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 claims description 5
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
229940114123 ferulate Drugs 0.000 claims description 4
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 4
230000002401 inhibitory effect Effects 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
150000004985 diamines Chemical class 0.000 claims description 3
230000007246 mechanism Effects 0.000 claims description 3
150000003254 radicals Chemical class 0.000 claims description 3
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 2
FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 claims description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
150000001450 anions Chemical class 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
239000004312 hexamethylene tetramine Substances 0.000 claims description 2
235000010299 hexamethylene tetramine Nutrition 0.000 claims description 2
125000005395 methacrylic acid group Chemical group 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
125000004429 atom Chemical group 0.000 claims 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
229960004011 methenamine Drugs 0.000 claims 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
239000000047 product Substances 0.000 description 15
239000003112 inhibitor Substances 0.000 description 14
238000003756 stirring Methods 0.000 description 13
239000000243 solution Substances 0.000 description 11
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
239000007864 aqueous solution Substances 0.000 description 7
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 7
238000001914 filtration Methods 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 5
239000007788 liquid Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000012258 stirred mixture Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000012065 filter cake Substances 0.000 description 4
150000002989 phenols Chemical class 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
239000013078 crystal Substances 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
238000007605 air drying Methods 0.000 description 2
150000001721 carbon Chemical group 0.000 description 2
238000001035 drying Methods 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
239000002198 insoluble material Substances 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
230000002028 premature Effects 0.000 description 2
238000000746 purification Methods 0.000 description 2
239000002002 slurry Substances 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
QIJIUJYANDSEKG-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-amine Chemical class CC(C)(C)CC(C)(C)N QIJIUJYANDSEKG-UHFFFAOYSA-N 0.000 description 1
DXCXWVLIDGPHEA-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-[(4-ethylpiperazin-1-yl)methyl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)CN1CCN(CC1)CC DXCXWVLIDGPHEA-UHFFFAOYSA-N 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
101100173542 Caenorhabditis elegans fer-1 gene Proteins 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
241000271317 Gonystylus bancanus Species 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
239000004327 boric acid Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000002704 decyl 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])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000004821 distillation Methods 0.000 description 1
125000003438 dodecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
UJHBVMHOBZBWMX-UHFFFAOYSA-N ferrostatin-1 Chemical compound NC1=CC(C(=O)OCC)=CC=C1NC1CCCCC1 UJHBVMHOBZBWMX-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
235000019157 thiamine Nutrition 0.000 description 1
150000003544 thiamines Chemical class 0.000 description 1
WEQHQGJDZLDFID-UHFFFAOYSA-J thorium(iv) chloride Chemical compound Cl[Th](Cl)(Cl)Cl WEQHQGJDZLDFID-UHFFFAOYSA-J 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/18—Bridged systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Cosmetics (AREA)
Polymerisation Methods In General (AREA)

JP58141974A 1982-08-04 1983-08-04 ｐ−ニトロソ−フエノ−ルのアミン塩及びその製造方法 Pending JPS5962552A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US40511382A	1982-08-04	1982-08-04
US405113		1982-08-04

Publications (1)

Publication Number	Publication Date
JPS5962552A true JPS5962552A (ja)	1984-04-10

Family

ID=23602329

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP58141974A Pending JPS5962552A (ja)	1982-08-04	1983-08-04	ｐ−ニトロソ−フエノ−ルのアミン塩及びその製造方法

Country Status (6)

Country	Link
JP (1)	JPS5962552A (it)
DE (1)	DE3326723A1 (it)
ES (1)	ES8502414A1 (it)
FR (1)	FR2531425A1 (it)
GB (1)	GB2126214A (it)
IT (1)	IT1168951B (it)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62187710A (ja) *	1986-02-14	1987-08-17	Kohjin Co Ltd	アクリルモノマ−用重合禁止剤

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5753714A (en) *	1987-02-03	1998-05-19	Merrell Pharmaceuticals Inc.	Polyamine derivatives

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1273598A (fr) *	1960-11-10	1961-10-13	Bayer Ag	Procédé de préparation de composés alcoylammoniums
US3842079A (en) *	1971-02-26	1974-10-15	J Michaelson	Nitroso aryloxy quaternary ammonium compounds
GB1601979A (en) *	1978-01-06	1981-11-04	Rohm & Haas	Polymerization inhibition
CA1139775A (en) *	1979-05-21	1983-01-18	Andrew C. Backus	Polymerization inhibitors
DE2931553A1 (de) *	1979-08-03	1981-02-26	Basf Ag	Verfahren zur stabilisierung monomerer acrylsaeureester gegen vorzeitige polymerisation

1983
- 1983-07-25 DE DE19833326723 patent/DE3326723A1/de not_active Withdrawn
- 1983-07-28 FR FR8312680A patent/FR2531425A1/fr active Pending
- 1983-07-29 GB GB08320554A patent/GB2126214A/en not_active Withdrawn
- 1983-08-02 IT IT22396/83A patent/IT1168951B/it active
- 1983-08-03 ES ES524715A patent/ES8502414A1/es not_active Expired
- 1983-08-04 JP JP58141974A patent/JPS5962552A/ja active Pending

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62187710A (ja) *	1986-02-14	1987-08-17	Kohjin Co Ltd	アクリルモノマ−用重合禁止剤

Also Published As

Publication number	Publication date
IT8322396A0 (it)	1983-08-02
ES524715A0 (es)	1985-01-01
IT8322396A1 (it)	1985-02-02
FR2531425A1 (fr)	1984-02-10
GB8320554D0 (en)	1983-09-01
ES8502414A1 (es)	1985-01-01
GB2126214A (en)	1984-03-21
DE3326723A1 (de)	1984-02-16
IT1168951B (it)	1987-05-20

Publication	Publication Date	Title
US2438091A (en)	1948-03-16	Aspartic acid esters and their preparation
Grimmel et al.	1946	Phosphazo compounds and their use in preparing amides
US3652671A (en)	1972-03-28	Process for making a cationic methacrylamide
JPH05194614A (ja)	1993-08-03	アクリル酸およびエステルの重合抑制剤
US3231601A (en)	1966-01-25	Process for the cyanoethylation of aromatic amines
JPS5962552A (ja)	1984-04-10	ｐ−ニトロソ−フエノ−ルのアミン塩及びその製造方法
US3714249A (en)	1973-01-30	Hydroxyalkylaminoalkylamides and their preparation
EP0246849B1 (en)	1991-01-30	Method of preparing n-acryloyl-alpha-amino acids
US3277175A (en)	1966-10-04	Preparation of p-nitrodiphenylamines
JPH07112986B2 (ja)	1995-12-06	カルボン酸クロライドの製法，およびその触媒
EP0775729A1 (en)	1997-05-28	Process for making aminoanthraquinone blue colourants
US4239886A (en)	1980-12-16	Salts of N-acylaminohydroxynaphthalenesulphonic acids
JPS601316B2 (ja)	1985-01-14	有機ゲルマニウム化合物
US2809984A (en)	1957-10-15	Cyanoethylated anilides and phenylene bis acid amides
US3121111A (en)	1964-02-11	Novel 4-thiohydantoic acids
JPS63166852A (ja)	1988-07-11	エステル基を含有するｎ−置換アクリルアミド
RU2070039C1 (ru)	1996-12-10	Бромзамещенные n-бензгидрил-n-(трифторацетил)мочевины, проявляющие противосудорожную активность, и способ их получения
JPS60132933A (ja)	1985-07-16	ニトロジアリ‐ルアミンの製造方法
US3180888A (en)	1965-04-27	Aminohaloboranes and preparation thereof
Chiriac et al.	2004	Synthesis of aromatic amides at room temperature using triphenyl phosphite-4-dimethylaminopyridine as reagent
USRE32952E (en)	1989-06-13	Method of preparing N-acryloyl-α-amino acids
PL93096B1 (it)	1977-05-30
JPS6284059A (ja)	1987-04-17	ジスルフイド化合物及びその製造方法
JPH02207077A (ja)	1990-08-16	ベンゾトリアゾール誘導体
JPH0627128B2 (ja)	1994-04-13	軸不斉を有する光学活性な重合用触媒

JPS5962552A - ｐ−ニトロソ−フエノ−ルのアミン塩及びその製造方法 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (1)

Family

ID=23602329

Family Applications (1)

Country Status (6)

Cited By (1)

Families Citing this family (1)

Family Cites Families (5)

Cited By (1)

Also Published As

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