| Name | 8-Bromooctanoic acid ethyl ester |
| Synonyms | ethyl 8-bromooctanoate ETHYL W-BROMOOCTANOATE ETHYL 8-BROMOOCTANOATE Ethyl 8-bromoocatanoate 8-Bromooctanoic Ethylester ETHYL OMEGA-BROMOOCTANOATE 8-CAPRYLIC ACID ETHYL ESTER 8-Bromooctanoic acid ethyl ester 8-BROMOOCTANOIC ACID ETHYL ESTER 8-BroMooCLanoic Acid Ethyl Ester 8-Bromo octanioic acid ethyl ester |
| CAS | 29823-21-0 |
| EINECS | 608-417-5 |
| InChI | InChI=1/C10H19BrO2/c1-2-13-10(12)8-6-4-3-5-7-9-11/h2-9H2,1H3 |
| Molecular Formula | C10H19BrO2 |
| Molar Mass | 251.16 |
| Density | 1.194 |
| Boling Point | 123°C/ 3mm |
| Flash Point | 139.5°C |
| Solubility | DMSO (Slightly), Ethyl Acetate (Slightly) |
| Vapor Presure | 0.00831mmHg at 25°C |
| Appearance | Oil |
| Color | Clear Colourless |
| Storage Condition | 2-8°C |
| Refractive Index | 1.462 |
| Hazard Symbols | Xi - Irritant![]() |
| Hazard Class | IRRITANT |
| LogP | 3.809 |
| introduction | 8-ethyl bromide is colorless to light yellow liquid. it is an excellent solvent and can also be used as an intermediate in medicine and pesticides. |
| Uses | Ethyl 8-bromooctanoate is a useful research reagent for organic synthesis and other chemical processes. |
| synthesis method | the synthesis steps of ethyl 8-bromooctanoate are as follows: S1 makes 1,6-dibromohexane and diethyl malonate undergo substitution reaction to obtain compound 2-(6-bromohexyl)-diethyl malonate; S2 makes the 2-(6-hexyl)-diethyl malonate undergo ester hydrolysis and decarboxylation reaction, 8-bromooctanoic acid; S3, the 8-bromooctanoic acid and absolute ethanol esterification reaction, to obtain 8-bromooctanoic acid ethyl ester. |