CAS 6000-00-6
:Metil (2E)-4-bromo-2-butenoato
- Crotonic acid, 4-bromo-, methyl ester, (E)-
- 2-Butenoic acid, 4-bromo-, methyl ester, (E)-
- 2-Butenoic acid, 4-bromo-, methyl ester, (2E)-
- Methyl (2E)-4-bromo-2-butenoate
- Methyl (E)-4-bromocrotonate
- METHYL 4-BROMOCROTONATE
- METHYL TRANS-4-BROMO-2-BUTENOATE
- 4-BROMOCROTONIC ACID METHYL ESTER
- TRANS-METHYL-4-BROMOCROTONATE
- (E)-4-Bromo-2-butenoic acid methyl ester
- TRANS-4-BROMO-2-BUTENOIC ACID METHYL ESTER
- TRANS-METHYL 4-BROMO-2-BUTENOATE, STAB.
- trans-Methyl-4-bromocrotonate, 97 %
- Methyl (E)-4-bromo-2-butenoate
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Methyl (E)-4-bromobut-2-enoate
CAS:Methyl (E)-4-bromobut-2-enoatePureza:90%Peso molecular:179.01g/molMethyl trans-4-Bromo-2-butenoate (>85%)
CAS:Producto controladoApplications Methyl trans-4-Bromo-2-butenoate is used as a reagent in the synthesis of several organic compounds including that of dimethoxy ketals and ketones via electrochemical oxidative decarboxylation of malonic acids.
References Ma, X., et al.: Org. Lett., 17, 4690 (2015);Fórmula:C5H7BrO2Pureza:>85%Forma y color:NeatPeso molecular:179.01Methyl trans-4-bromo-2-butenoate
CAS:Methyl trans-4-bromo-2-butenoate is a synthetic compound that contains a hydroxyl group and two bromine atoms. It is synthesized by the reaction of diethyl succinate, hydrogen, and piperazine in an aqueous solution. Methyl trans-4-bromo-2-butenoate has been shown to have antineoplastic activity in combination with epidermal growth factor (EGF) and carbohydrate conjugates. It also binds to cell surface receptors on the epidermal cells, inhibiting their growth. The structural formula of methyl trans-4-bromo-2-butenoate can be seen below: [[File:Methyltrans4bromobutanoate.png|thumb|300px|left|The structural formula of methyl trans-[4] -[bromo]-[2] -butenoate.]]
Fórmula:C5H7BrO2Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:179.01 g/mol


