- Ethyl oxalyl monochloride
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- $8.00 / 1KG
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2024-01-22
- CAS:4755-77-5
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | Ethyl chlorooxoacetate Basic information | | Uses |
| Product Name: | Ethyl chlorooxoacetate | | Synonyms: | Monoethyl oxalyl chloride;Ethyl chloroglyoxylate~Oxalic acid monoethyl ester chloride;ETHYL CHLOROOXOACETATE,98%;Ethyloxalylchloride,98%;Ethyl chloroglyoxylate, mono-Ethyl oxalyl chloride, Monoethyl oxalyl chloride, Oxalic acid monoethyl ester chloride;Ethyl chloroglyoxylate, Monoethyl oxalyl chloride, Oxalic acid monoethyl ester chloride;2-Oxo-2-chloroacetic acid ethyl ester;Chloroformylformic acid ethyl | | CAS: | 4755-77-5 | | MF: | C4H5ClO3 | | MW: | 136.53 | | EINECS: | 225-285-0 | | Product Categories: | Organics;Pharmaceutical Intermediates;Indoles;bc0001 | | Mol File: | 4755-77-5.mol |  |
| | Ethyl chlorooxoacetate Chemical Properties |
| | Ethyl chlorooxoacetate Usage And Synthesis |
| Uses | Ethyl oxalyl monochloride is used in the synthesis of 2-oxo-3-alkenoic esters and alpha-keto ester in good yield. Ethyl oxalyl monochloride acts as a reactant in the preparation of oxyoxalamide derivatives as an epoxide hydrolase inhibitor.
| | Description | Ethyl chlorooxoacetate has been used as a reactant in the preparation of oxyoxalamide derivatives as epoxide hydrolase inhibitors. | | Chemical Properties | clear liquid | | Uses | Ethyl chlorooxoacetate can be used for the synthesis of:
- α-keto esters.
- Functionalized 3-pyrolin-2-ones.
- Substituted arylglyoxylic acids via Friedel–Crafts acylation.
- Substituted 9,10-phenanthrenequinones.
- Quinoxalinone derivatives.
| | Uses | Ethyl oxalyl chloride is used in the synthesis of 2-oxo-3-alkenoic esters and alpha-keto ester in good yield. It acts as a reactant in the preparation of oxyoxalamide derivatives as an epoxide hydrolase inhibitor. |
| | Ethyl chlorooxoacetate Preparation Products And Raw materials |
| Preparation Products | ETHYL 3,4-DIHYDRO-6-METHYL-4-OXOTHIENO[2,3-D]PYRIMIDINE-2-CARBOXYLATE-->2-(5-BROMO-2-THIENYL)-3-CHLOROQUINOXALINE-->Oxamic acid sodium salt-->N1-(2,4-DIMETHOXYBENZYL)-N2-(2-PYRIDIN-2-YL)ETHYL)OXALAMIDE-->Oxamic acid-->Ethyl 5-Methyl-1,3,4-thiadiazole-2-carboxylate-->ETHYL THIOPHENE-2-GLYOXYLATE-->Ethyl-4-Chloroindole-2-Carboxylate-->1,3-Bis(4-bromophenyl)propanone-->N-OXALYL GLYCINE-->Ethyl 2-hydroxyisobutyrate-->Ethyl benzoylformate-->Ethyl [(5-nitro-1,3-thiazol-2-yl)amino](oxo)acetate-->2-CARBETHOXY-5,7-DIHYDROXY-4'-METHOXYISOFLAVONE-->3-(4-methylphenyl)-1,2,4-Oxadiazole-5-carboxylic acid ethyl ester-->N-(2-Ethoxy-phenyl)-oxalamic acid ethyl ester |
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