GB1234571A - - Google Patents
Info
- Publication number
- GB1234571A GB1234571A GB1234571DA GB1234571A GB 1234571 A GB1234571 A GB 1234571A GB 1234571D A GB1234571D A GB 1234571DA GB 1234571 A GB1234571 A GB 1234571A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- carboxylic acid
- compound
- phenol
- glycidyl
- 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
- -1 Epoxide esters Chemical class 0.000 abstract 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 5
- 150000001412 amines Chemical group 0.000 abstract 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- PCAXITAPTVOLGL-UHFFFAOYSA-N 2,3-diaminophenol Chemical class NC1=CC=CC(O)=C1N PCAXITAPTVOLGL-UHFFFAOYSA-N 0.000 abstract 1
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 abstract 1
- NBGAYCYFNGPNPV-UHFFFAOYSA-N 2-aminooxybenzoic acid Chemical class NOC1=CC=CC=C1C(O)=O NBGAYCYFNGPNPV-UHFFFAOYSA-N 0.000 abstract 1
- NDACNGSDAFKTGE-UHFFFAOYSA-N 3-hydroxydiphenylamine Chemical compound OC1=CC=CC(NC=2C=CC=CC=2)=C1 NDACNGSDAFKTGE-UHFFFAOYSA-N 0.000 abstract 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 1
- HUNAOMMDPVTQEY-UHFFFAOYSA-N CCCCC1=CC(O)=C(C)C(C)=C1N.Br Chemical compound CCCCC1=CC(O)=C(C)C(C)=C1N.Br HUNAOMMDPVTQEY-UHFFFAOYSA-N 0.000 abstract 1
- OIWYAIBSNUMQJR-UHFFFAOYSA-N CCCCCCCCCCCCC1=CC2=CC=CC=C2N=C1O.Cl Chemical compound CCCCCCCCCCCCC1=CC2=CC=CC=C2N=C1O.Cl OIWYAIBSNUMQJR-UHFFFAOYSA-N 0.000 abstract 1
- PIPSKZIJMANDMD-UHFFFAOYSA-N N-[2-(dimethylamino)phenyl]-N-phenylhydroxylamine Chemical compound CN(C)C1=C(C=CC=C1)N(C1=CC=CC=C1)O PIPSKZIJMANDMD-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000010494 dissociation reaction Methods 0.000 abstract 1
- 230000005593 dissociations Effects 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid group Chemical class C(CCCCCC)(=O)O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 150000004806 hydroxypyridines Chemical class 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical group 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- OHOJEXXPXGPKHM-UHFFFAOYSA-N oxiran-2-ylmethyl heptanoate Chemical compound CCCCCCC(=O)OCC1CO1 OHOJEXXPXGPKHM-UHFFFAOYSA-N 0.000 abstract 1
- OVUDDTWGFUTRSK-UHFFFAOYSA-N oxiran-2-ylmethyl undec-10-enoate Chemical compound C=CCCCCCCCCC(=O)OCC1CO1 OVUDDTWGFUTRSK-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 abstract 1
- 125000003367 polycyclic group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- FNXKBSAUKFCXIK-UHFFFAOYSA-M sodium;hydrogen carbonate;8-hydroxy-7-iodoquinoline-5-sulfonic acid Chemical class [Na+].OC([O-])=O.C1=CN=C2C(O)=C(I)C=C(S(O)(=O)=O)C2=C1 FNXKBSAUKFCXIK-UHFFFAOYSA-M 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/16—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by esterified hydroxyl radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR108440A FR1532542A (fr) | 1967-05-30 | 1967-05-30 | Procédé de synthèse d'esters époxydés |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1234571A true GB1234571A (cg-RX-API-DMAC10.html) | 1971-06-03 |
Family
ID=8631947
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1234571D Expired GB1234571A (cg-RX-API-DMAC10.html) | 1967-05-30 | 1968-05-28 |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE715803A (cg-RX-API-DMAC10.html) |
| FR (1) | FR1532542A (cg-RX-API-DMAC10.html) |
| GB (1) | GB1234571A (cg-RX-API-DMAC10.html) |
| LU (1) | LU56148A1 (cg-RX-API-DMAC10.html) |
| NL (1) | NL6807443A (cg-RX-API-DMAC10.html) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001030881A1 (en) * | 1999-10-27 | 2001-05-03 | Shell Internationale Research Maatschappij B.V. | Process for glycidation of carboxylic acids |
-
1967
- 1967-05-30 FR FR108440A patent/FR1532542A/fr not_active Expired
-
1968
- 1968-05-27 LU LU56148D patent/LU56148A1/xx unknown
- 1968-05-27 NL NL6807443A patent/NL6807443A/xx unknown
- 1968-05-28 BE BE715803D patent/BE715803A/xx unknown
- 1968-05-28 GB GB1234571D patent/GB1234571A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001030881A1 (en) * | 1999-10-27 | 2001-05-03 | Shell Internationale Research Maatschappij B.V. | Process for glycidation of carboxylic acids |
Also Published As
| Publication number | Publication date |
|---|---|
| LU56148A1 (cg-RX-API-DMAC10.html) | 1968-09-11 |
| BE715803A (cg-RX-API-DMAC10.html) | 1968-10-16 |
| FR1532542A (fr) | 1968-07-12 |
| NL6807443A (cg-RX-API-DMAC10.html) | 1968-12-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1372537A (en) | Preparation of carbamates | |
| GB1304667A (cg-RX-API-DMAC10.html) | ||
| GB1247370A (en) | Glyoxals and production thereof | |
| GB1188185A (en) | Preparation of d-2-Amino-1-Butanol | |
| GB1188791A (en) | Olefin Oxides | |
| GB1182405A (en) | Process for Preparing Sarcosinonitrile | |
| ES406745A1 (es) | Procedimiento para la fabricacion de esteres alquilicos de acidos carboxilicos. | |
| GB1324257A (en) | Nitrolotrisalkylene-tris-triidoisophthalamic acid compounds particularly for use as radiopaque agents | |
| GB1182815A (en) | New Salts of N-Carbamyl-Glutamic Acid and of N-Carbamyl-Aspartic Acid. | |
| GB1143589A (en) | Process for the preparation of 2-amino-4-hydroxytoluene | |
| ES356415A1 (es) | Procedimiento para la preparacion de di (aminofenil) meta- no. | |
| GB1174535A (en) | Substituted Phenylacetic acids and process of preparation thereof | |
| GB1385148A (en) | Process for preparing alkyl or cycloalkyl nitroacetoacetates | |
| GB1311548A (en) | Preparation of 4-alkoxy-3-nitro benzoic acids and their salts and the corresponding 2-aminoethylnitrobehzoates and 2-aminoethyl aminobenzoates | |
| GB1450611A (en) | Process for the production of acetonin | |
| GB1471575A (en) | Stabilized ethylenically unsaturated beta-hydroxy esters | |
| GB1147832A (en) | Fluorene xanthene and thioxanthene derivatives | |
| GB1212760A (en) | Preparation of salts of alkyl hydroxymethylene malonates | |
| NL6907904A (cg-RX-API-DMAC10.html) | ||
| GB1252779A (cg-RX-API-DMAC10.html) | ||
| GB1324740A (en) | Methanesulphonic acid aryl ester process for their preparation and their nematocidal use | |
| GB1251340A (cg-RX-API-DMAC10.html) | ||
| JPS5463077A (en) | Preparation of imidazoline derivative | |
| GB572931A (en) | Improvements in or relating to the preparation of nitro-guanidine | |
| GB1221238A (en) | 0-ethyl threonine and its derivatives |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |