GB1328232A - Carbamic acid derivatives - Google Patents
Carbamic acid derivativesInfo
- Publication number
- GB1328232A GB1328232A GB5046770A GB5046770A GB1328232A GB 1328232 A GB1328232 A GB 1328232A GB 5046770 A GB5046770 A GB 5046770A GB 5046770 A GB5046770 A GB 5046770A GB 1328232 A GB1328232 A GB 1328232A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid derivatives
- carbamic acid
- triacrylate
- dimethacrylate
- oligomers
- 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
- 150000004657 carbamic acid derivatives Chemical class 0.000 title abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 239000012948 isocyanate Substances 0.000 abstract 2
- 150000002513 isocyanates Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- GQPVFBDWIUVLHG-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(CO)COC(=O)C(C)=C GQPVFBDWIUVLHG-UHFFFAOYSA-N 0.000 abstract 1
- CQHKDHVZYZUZMJ-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-prop-2-enoyloxypropyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(CO)COC(=O)C=C CQHKDHVZYZUZMJ-UHFFFAOYSA-N 0.000 abstract 1
- JUDXBRVLWDGRBC-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(COC(=O)C(C)=C)COC(=O)C(C)=C JUDXBRVLWDGRBC-UHFFFAOYSA-N 0.000 abstract 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- -1 cycloaliphatic Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005056 polyisocyanate Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
-
- 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
- C08F20/20—Esters of polyhydric alcohols or polyhydric phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1328232 Carbamic acid derivatives SUN CHEMICAL CORP 10 Aug 1970 [15 Aug 1969] 50467/71 Divided out of 1328231 Heading C2C The invention comprises the product of reacting a free-hydroxyl containing polyethylenically unsaturated ester of an aliphatic polyhydric alcohol and acrylic, methacrylic or itaconic acid with an organic isocyanate, and oligomers thereof. Preferred esters are pentaerythritol diacrylate, triacrylate, dimethacrylate, trimethacrylate and di-itaconate; dipentaerythritol diacrylate, triacrylate, tetraacrylate, pentaacrylate, dimethacrylate, tetramethacrylate, trisitaconate and pentaitaconate and mixtures and oligomers thereof. Suitable isocyanates include aliphatic, cycloaliphatic, heterocyclic and aromatic mono- and poly-isocyanates and mixtures thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85063369A | 1969-08-15 | 1969-08-15 | |
| GB3939970A GB1318302A (en) | 1969-08-16 | 1970-08-10 | Registering of blood pulses |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1328232A true GB1328232A (en) | 1973-08-30 |
Family
ID=26264090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5046770A Expired GB1328232A (en) | 1969-08-15 | 1970-08-10 | Carbamic acid derivatives |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1328232A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0264551A3 (en) * | 1986-07-25 | 1988-11-17 | Bayer Ag | Methacrylic-acid derivatives containing urethane groups |
| US4935535A (en) * | 1989-01-19 | 1990-06-19 | National Science Council | Ultraviolet-autocurable benzophenone tetracarboxylic dianhydride-based polyurethane acrylate oligomers |
-
1970
- 1970-08-10 GB GB5046770A patent/GB1328232A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0264551A3 (en) * | 1986-07-25 | 1988-11-17 | Bayer Ag | Methacrylic-acid derivatives containing urethane groups |
| US4879402A (en) * | 1986-07-25 | 1989-11-07 | Bayer Aktiengesellschaft | (Methyl)acrylic acid derivatives containing urethane groups |
| US4952241A (en) * | 1986-07-25 | 1990-08-28 | Bayer Aktiengesellschaft | (Meth)acylic acid derivatives containing urethane groups |
| US4935535A (en) * | 1989-01-19 | 1990-06-19 | National Science Council | Ultraviolet-autocurable benzophenone tetracarboxylic dianhydride-based polyurethane acrylate oligomers |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| UA7217A1 (en) | Continuous process for the production of organic isocyanates | |
| ES8301663A1 (en) | Microencapsulation process | |
| NO304653B1 (en) | Bile acid derivatives, drugs containing them and the use of compounds | |
| FI49727C (en) | A process for preparing polyurethanes from a polyisocyanate and a polyol component which is the reaction product of a fatty acid or fatty acid ester and a dialkanol mine. | |
| GB1415378A (en) | Photopolymerisable compositions and elements | |
| EP0035342A3 (en) | Goods display system | |
| ZA792366B (en) | Enzymic microbiological process for producing optically active aminoacids starting from hydanthoins and/or recemic carbamoyl derivatives | |
| ES384542A1 (en) | Substituted norbornyl and nortricyclyl derivatives and their use in perfumery | |
| GB1328232A (en) | Carbamic acid derivatives | |
| ES8705495A1 (en) | Transesterification process. | |
| CA2115050A1 (en) | Synthetic trnas | |
| Smith et al. | Loss of gene repression activity: a theory of cellular senescence | |
| EP0016402A3 (en) | Refrigerator | |
| GB1240622A (en) | Molluscicides | |
| JPS6433370A (en) | Stabilizing and refuge device for multistoried building | |
| ATE166642T1 (en) | 9-CHLORINE-PROSTAGLANDIN ESTERS AND AMIDES AND THEIR USE FOR THE PRODUCTION OF MEDICINAL PRODUCTS | |
| GB1263360A (en) | Process for recovering noble metals from supported catalysts | |
| AU1381388A (en) | Microspore-based selection system and products thereof | |
| EP0312803A3 (en) | Process and apparatus for conditioning bulk material | |
| JPS5778414A (en) | Production of urethane acrylate oligomer or urethane methacrylate oligomer and photopolymer composition therefrom | |
| GB1554362A (en) | Manufacture of isocyanates from substituted ureas | |
| GB1231649A (en) | ||
| Kontris et al. | Dynamics of the phytocenoses development of the submountain beech forest stands. I. phytocenoses | |
| HUT54148A (en) | Process for producing oxazolone compounds and pharmaceutical compositions comprising such compounds | |
| GB1238725A (en) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |