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| 4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER Basic information |
Product Name: | 4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER | Synonyms: | 4,4,4-TRICHLOROACETIC ACID ETHYL ESTER;4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER;ETHYL 4,4,4-TRICHLOROACETOACETATE;ethyl 4,4,4-trichloro-3-oxobutyrate;4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER, 97+%;4,4,4-trichloro-3-keto-butyric acid ethyl ester;ethyl 4,4,4-trichloro-3-oxobutanoate;ethyl 4,4,4-trichloro-3-oxo-butanoate | CAS: | 3702-98-5 | MF: | C6H7Cl3O3 | MW: | 233.48 | EINECS: | 223-041-8 | Product Categories: | C6 to C7;Carbonyl Compounds;Esters | Mol File: | 3702-98-5.mol | |
| 4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER Chemical Properties |
Melting point | 126-127.5 °C(Solv: ligroine (8032-32-4)) | Boiling point | 224-226 °C (lit.) | density | 1.389 g/mL at 20 °C (lit.) | refractive index | n20/D 1.470 | form | clear liquid | pka | 7.95±0.46(Predicted) | color | Colorless to Almost colorless | BRN | 1779520 |
Safety Statements | 23-24/25 | WGK Germany | 3 | HS Code | 2918.30.9000 |
| 4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER Usage And Synthesis |
Uses | Ethyl 4,4,4-Trichloro-3-oxobutanoate is a reagent used in the sunthesis of heterocyclic compounds. | Synthesis Reference(s) | The Journal of Organic Chemistry, 31, p. 3369, 1966 DOI: 10.1021/jo01348a060 |
| 4,4,4-TRICHLOROACETOACETIC ACID ETHYL ESTER Preparation Products And Raw materials |
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