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Ethyl 2-bromo-3-methylbutyrate

  • Product Name: Ethyl 2-bromo-3-methylbutyrate
  • CasNo: 609-12-1
  • Purity:
  • Appearance: clear colorless liquid

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CasNo: 609-12-1

Molecular Formula: C7H13BrO2

Appearance: clear colorless liquid

Factory Sells Best Quality Ethyl 2-bromo-3-methylbutyrate 609-12-1 with GMP standards

  • Molecular Formula:C7H13BrO2
  • Molecular Weight:209.083
  • Appearance/Colour:clear colorless liquid 
  • Vapor Pressure:0.751mmHg at 25°C 
  • Refractive Index:1.4485-1.4505  
  • Boiling Point:184 °C at 760 mmHg 
  • Flash Point:72.5 °C 
  • PSA:26.30000 
  • Density:1.294 g/cm3 
  • LogP:1.96900 

Ethyl 2-bromo-3-methylbutyrate(Cas 609-12-1) Usage

InChI:InChI=1/C7H13BrO2/c1-4-10-7(9)6(8)5(2)3/h5-6H,4H2,1-3H3/t6-/m0/s1

609-12-1 Relevant articles

Synthesis of α-alkylated γ-butyrolactones with concomitant anhydride kinetic resolution using a sulfamide-based catalyst

Claveau, Romain,Twamley, Brendan,Connon, Stephen J.

supporting information, p. 7574 - 7578 (2018/11/02)

The Kinetic Resolution (KR) of α-alkylat...

CARBAZOLE DERIVATIVE, SOLVATE THEREOF, OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF

-

Page/Page column 42, (2010/11/28)

An object of the present invention is to...

Pyrimidine acyclonucleoside derivatives, preparation method and use thereof

-

Page/Page column 15-16, (2010/02/12)

The invention relates to a compound havi...

Syntheses based on monocarbon molecules: II. Synthesis of ethyl isovalerate by isobutene carbonylation with carbon monoxide and ethanol in the presence of phosphine palladium complexes. Ethyl α-bromoisovalerate

Suerbaev,Abyzbekova,Shalmagambetov,Zhubanov

, p. 516 - 517 (2007/10/03)

Optimal conditions for the synthesis of ...

609-12-1 Process route

ethanol
64-17-5

ethanol

2-bromoisovaleric acid
10323-40-7,565-74-2

2-bromoisovaleric acid

ethyl 2-bromoisovalerate
609-12-1

ethyl 2-bromoisovalerate

Conditions
Conditions Yield
With sulfuric acid; for 16h; Reflux;
92%
With sulfuric acid; for 2h; Heating;
81%
With sulfuric acid; In benzene; for 48h; Heating;
80%
With sulfuric acid; for 36h; Heating / reflux;
55%
With sulfuric acid;
1,1-Dichloro-3-methyl-1-butene
32363-91-0

1,1-Dichloro-3-methyl-1-butene

ethyl 2-bromoisovalerate
609-12-1

ethyl 2-bromoisovalerate

Conditions
Conditions Yield
With methanesulfonic acid; bromine; chlorine; In ethanol;

609-12-1 Upstream products

  • 26464-05-1
    26464-05-1

    2-bromo-3-methyl-butyryl bromide

  • 64-17-5
    64-17-5

    ethanol

  • 10323-40-7
    10323-40-7

    2-bromoisovaleric acid

  • 503-74-2
    503-74-2

    3-methylbutyric acid

609-12-1 Downstream products

  • 63403-11-2
    63403-11-2

    α-m-tolyloxy-isovaleric acid

  • 63403-10-1
    63403-10-1

    α-m-tolyloxy-isovaleric acid ethyl ester

  • 63403-07-6
    63403-07-6

    α-p-tolyloxy-isovaleric acid

  • 63403-09-8
    63403-09-8

    α-p-tolyloxy-isovaleric acid ethyl ester

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