- Ethyl 4-bromocrotonate
-
- $0.00 / 1KG
-
2026-01-30
- CAS:37746-78-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 20 mt
|
| | Ethyl 4-bromocrotonate Basic information |
| | Ethyl 4-bromocrotonate Chemical Properties |
| Boiling point | 94-95 °C/12 mmHg (lit.) | | density | 1.402 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.493(lit.) | | Fp | 207 °F | | storage temp. | 2-8°C | | solubility | Chloroform (Sparingly), Methanol (Slightly) | | form | Liquid | | Specific Gravity | 1.402 | | color | Clear light yellow to brown | | Water Solubility | Insoluble in water. | | BRN | 1721388 | | Stability: | Light Sensitive | | InChI | 1S/C6H9BrO2/c1-2-9-6(8)4-3-5-7/h3-4H,2,5H2,1H3/b4-3+ | | InChIKey | FHGRPBSDPBRTLS-ONEGZZNKSA-N | | SMILES | CCOC(=O)\C=C\CBr | | CAS DataBase Reference | 37746-78-4(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Butenoic acid, 4-bromo-, ethyl ester, (E)-(37746-78-4) |
| Hazard Codes | C,Xi | | Risk Statements | 34-36/37/38 | | Safety Statements | 26-36/37/39-45-24/25 | | RIDADR | UN 3265 8/PG 2 | | WGK Germany | 3 | | F | 10-19-23 | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29161995 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Skin Corr. 1B |
| | Ethyl 4-bromocrotonate Usage And Synthesis |
| Chemical Properties | clear yellow liquid | | Uses | Ethyl 4-bromocrotonate is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs. | | Synthesis | General procedure for the synthesis of ethyl (E)-4-bromobut-2-enoate from ethyl crotonate: To a round-bottomed flask containing ethyl (2E)-but-2-enoate (10.9 g, 87.6 mmol) and carbon tetrachloride (100 mL), N-bromosuccinimide (NBS, 17 g, 96 mmol) and azobisisobutyronitrile (AIBN, 4.3 g, 26 mmol). The reaction mixture was stirred at 80 °C for 12 hours. After completion of the reaction, the reaction mixture was diluted with dichloromethane (DCM) and washed sequentially with saturated sodium bicarbonate solution, water and brine. The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent to give ethyl (E)-4-bromobut-2-enoate (7.5 g, 44% yield) as an oil. | | References | [1] Journal of the American Chemical Society, 2001, vol. 123, # 21, p. 4966 - 4973
[2] Patent: WO2017/100668, 2017, A1. Location in patent: Page/Page column 150
[3] Patent: WO2018/103058, 2018, A1. Location in patent: Page/Page column 150
[4] Bulletin de la Societe Chimique de France, 1966, p. 1315 - 1324
[5] Journal of Organometallic Chemistry, 1973, vol. 60, p. 209 - 217 |
| | Ethyl 4-bromocrotonate Preparation Products And Raw materials |
|