1-Bromo-3-methyl-2-butanone

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Products Intro: Product Name:1-Bromo-3-methyl-2-butanone
CAS:19967-55-6
Purity:99% Package:1kg;30USD|1000kg;0.5USD
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CAS:19967-55-6
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Company Name: Nanjing ChemLin Chemical Industry Co., Ltd.
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CAS:19967-55-6
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Products Intro: Product Name:1-Bromo-3-methylbutan-2-one
CAS:19967-55-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-24041

1-Bromo-3-methyl-2-butanone manufacturers

  • 1-Bromo-3-methyl-2-butanone
  • 1-Bromo-3-methyl-2-butanone pictures
  • $30.00 / 1kg
  • 2025-09-25
  • CAS:19967-55-6
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
1-Bromo-3-methyl-2-butanone Basic information
Product Name:1-Bromo-3-methyl-2-butanone
Synonyms:1-BROMO-3-METHYL-2-BUTANONE;Bromomethyl isopropyl ketone;Isopropyl bromomethyl ketone;2-Butanone, 1-bromo-3-methyl-;1-Bromo-3-methylbutan-2-one;1-BroMo-3,3-diMethyl-2-propanone;2-BroMo-1-isopropylethanone;1-BroMo-3-Methylbutan-2-one, 95+%
CAS:19967-55-6
MF:C5H9BrO
MW:165.03
EINECS:
Product Categories:
Mol File:19967-55-6.mol
1-Bromo-3-methyl-2-butanone Structure
1-Bromo-3-methyl-2-butanone Chemical Properties
Boiling point 164 °C
density 1.355
refractive index 1.4685
Fp 56 °C
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility Chloroform, Ethyl Acetate
form Oil
color Clear Colourless
Safety Information
HS Code 2914120000
MSDS Information
1-Bromo-3-methyl-2-butanone Usage And Synthesis
Synthesis
3-Methyl-2-butanone

563-80-4

1-Bromo-3-methyl-2-butanone

19967-55-6

Example 1 Synthesis of 1-bromo-3-methylbutan-2-one: (1) Bromine (12.9 mL, 250 mmol) was added slowly and dropwise to an ethanol (EtOH, 250 mL) solution of 3-methyl-2-butanone (25.8 g, 300 mmol) under ice bath cooling conditions. The reaction mixture was stirred continuously for 2 h in an ice bath. After completion of the reaction, it was diluted by adding petroleum ether (600 mL). The organic phase was separated and washed twice with distilled water. The combined aqueous phases were back-extracted twice with petroleum ether. All organic phases were combined and washed twice each with cold sodium carbonate solution and saturated saline in that order. The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure at room temperature to afford the target product 1-bromo-3-methylbutan-2-one in 50% yield.

References[1] Patent: US5910506, 1999, A
[2] Patent: WO2007/14921, 2007, A1. Location in patent: Page/Page column 69
[3] Patent: WO2003/106455, 2003, A1. Location in patent: Page 60
[4] Patent: WO2007/14922, 2007, A1. Location in patent: Page/Page column 79-80
[5] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 8, p. 2922 - 2926
Tag:1-Bromo-3-methyl-2-butanone(19967-55-6) Related Product Information
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