GB1428454A - Oligourethaneacrylates mehtods for their manufacture and polymers on the basis thereof - Google Patents
Oligourethaneacrylates mehtods for their manufacture and polymers on the basis thereofInfo
- Publication number
- GB1428454A GB1428454A GB699973A GB699973A GB1428454A GB 1428454 A GB1428454 A GB 1428454A GB 699973 A GB699973 A GB 699973A GB 699973 A GB699973 A GB 699973A GB 1428454 A GB1428454 A GB 1428454A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- formula
- divalent
- trivalent
- groups
- Prior art date
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- 229920000642 polymer Polymers 0.000 title 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 230000003797 telogen phase Effects 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- 229910005965 SO 2 Inorganic materials 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000732 arylene group Chemical group 0.000 abstract 1
- IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical group C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- -1 dimethyl-substituted phenylene groups Chemical group 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- 125000001033 ether group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 229920000768 polyamine Polymers 0.000 abstract 1
- 229920005862 polyol Polymers 0.000 abstract 1
- 150000003077 polyols Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
- C08F20/36—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate containing oxygen in addition to the carboxy oxygen, e.g. 2-N-morpholinoethyl (meth)acrylate or 2-isocyanatoethyl (meth)acrylate
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1428454 Oligourethanacrylates ORDENA LENINA INST KHIMICHE FIZIKI AKAD NAUK SSSR and CHERNORECHEN DVAZHDY ORDENA TRUDO KRAS ZNAME KHIMICHE KOMBINAT IM MI KALININA OBLAST GORKOVSKAYA DZERZHINSK USSR 13 Feb 1973 6999/73 Heading C2C [Also in Division C3] Novel oligourethanacrylates having the general Formula I in which X is a hydrogen or halogen atom or a methyl group; R is an alkylene or arylene group; p is an integer and is 2 or 3 or 4 depending on the valency of R<SP>1</SP>: and U is a urethane group of Formula V or VIII in which Y is hydrogen or an aryl group and Z is hydrogen, an alkyl or an aryl group; R<SP>1</SP> is a divalent, trivalent or tetravalent group, the said divalent group being selected from alkylene groups of from 2 to 10 carbon atoms, phenylene groups, dimethyl-substituted phenylene groups, a diphenylene group, the group of Formula XI in which M is CH 2 , O, S, SO 2 , NH or (CH 3 ) 2 C, divalent aliphatic groups containing one or two ether groups or an ester group, the said trivalent group being a trivalent aliphatic hydrocarbon group, and the said tetravalent group being a tetravalent aliphatic hydrocarbon group or the group of Formula XII where M<SP>1</SP> is a methylene group or an oxygen atom; optionally the group R<SP>1</SP> may be an oligomeric group of formula in which R<SP>11</SP> is any one of the divalent groups defined above in respect of R<SP>1</SP>, R<SP>111</SP> is one of the divalent or trivalent groups defined above in respect of R<SP>1</SP>, n is an integer of 1 to 5 when R<SP>111</SP> is divalent and n is 1 when R<SP>111</SP> is trivalent, are prepared by reacting a polyol polychloroformate with a telogen of Formula (IV), or reacting a polyamine with a telogen of Formula (III) in an organic solvent medium in the presence of a hydrogen chloride acceptor and at a temperature of from - 10‹ C. to the boiling point of the solvent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB699973A GB1428454A (en) | 1973-02-13 | 1973-02-13 | Oligourethaneacrylates mehtods for their manufacture and polymers on the basis thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB699973A GB1428454A (en) | 1973-02-13 | 1973-02-13 | Oligourethaneacrylates mehtods for their manufacture and polymers on the basis thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1428454A true GB1428454A (en) | 1976-03-17 |
Family
ID=9824701
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB699973A Expired GB1428454A (en) | 1973-02-13 | 1973-02-13 | Oligourethaneacrylates mehtods for their manufacture and polymers on the basis thereof |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1428454A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0183119A1 (en) * | 1984-11-12 | 1986-06-04 | AUSCHEM S.p.A. | Polymers based on ethylenically unsaturated monomers modified with oligourethanes and aqueous dispersions obtained therefrom |
| US5276068A (en) * | 1985-03-29 | 1994-01-04 | Jeneric/Pentron, Inc. | Dental resin materials |
| US5969000A (en) * | 1997-01-17 | 1999-10-19 | Jeneric Pentron Incorporated | Dental resin materials |
| US6345984B2 (en) | 1998-04-13 | 2002-02-12 | Jeneric/Pentron, Inc. | Prefabricated components for dental appliances |
| US7255562B2 (en) | 1999-01-08 | 2007-08-14 | 3M Innovative Properties Company | Dental mill blanks |
-
1973
- 1973-02-13 GB GB699973A patent/GB1428454A/en not_active Expired
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0183119A1 (en) * | 1984-11-12 | 1986-06-04 | AUSCHEM S.p.A. | Polymers based on ethylenically unsaturated monomers modified with oligourethanes and aqueous dispersions obtained therefrom |
| US5276068A (en) * | 1985-03-29 | 1994-01-04 | Jeneric/Pentron, Inc. | Dental resin materials |
| US5444104A (en) * | 1985-03-29 | 1995-08-22 | Jeneric/Pentron, Inc. | Dental resin materials |
| US5969000A (en) * | 1997-01-17 | 1999-10-19 | Jeneric Pentron Incorporated | Dental resin materials |
| US6846181B2 (en) | 1997-12-29 | 2005-01-25 | Pentron Corporation | Prefabricated components for dental appliances |
| US6345984B2 (en) | 1998-04-13 | 2002-02-12 | Jeneric/Pentron, Inc. | Prefabricated components for dental appliances |
| US7255562B2 (en) | 1999-01-08 | 2007-08-14 | 3M Innovative Properties Company | Dental mill blanks |
| US7845947B2 (en) | 1999-01-08 | 2010-12-07 | 3M Innovative Properties Company | Dental mill blanks |
| US8317516B2 (en) | 1999-01-08 | 2012-11-27 | 3M Innovative Properties Company | Dental mill blanks |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |