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1-Bromo-5-hexanone

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1-Bromo-5-hexanone manufacturers

  • 1-BROMO-5-HEXANONE
  • 1-BROMO-5-HEXANONE pictures
  • 2026-07-21
  • CAS:10226-29-6
  • Min. Order: 1kg
  • Purity: 0.95
  • Supply Ability: 20tons
  • 1-Bromo-5-hexanone
  • 1-Bromo-5-hexanone pictures
  • 2026-06-30
  • CAS:10226-29-6
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 10000KGS
  • 6-Bromohexan-2-one
  • 6-Bromohexan-2-one pictures
  • 2023-10-22
  • CAS:10226-29-6
  • Min. Order: 1drums
  • Purity: 99%min.
  • Supply Ability: 10tons
1-Bromo-5-hexanone Basic information
Product Name:1-Bromo-5-hexanone
Synonyms:6-Bromhexan-2-on;1-bromo-5-hexanone;4-Bromobutyl methyl ketone;5-Oxohexyl BroMide;2-Hexanone, 6-bromo-;6-Bromohexan-2-on;6-Bromohexan-2-one
CAS:10226-29-6
MF:C6H11BrO
MW:179.05
EINECS:233-544-4
Product Categories:Aliphatics;Miscellaneous Reagents
Mol File:10226-29-6.mol
1-Bromo-5-hexanone Structure
1-Bromo-5-hexanone Chemical Properties
Boiling point 216°C (rough estimate)
density 1.3494
refractive index 1.4890 (estimate)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility soluble in Chloroform
form Oil
color Colourless
CAS DataBase Reference10226-29-6(CAS DataBase Reference)
Safety Information
MSDS Information
1-Bromo-5-hexanone Usage And Synthesis
Chemical PropertiesColourless Oil
Uses6-Bromo-2-hexanone (cas# 10226-29-6) is a compound useful in organic synthesis.
Synthesis
1-Methylcyclopentanol

1462-03-9

1-Bromo-5-hexanone

10226-29-6

The general procedure for the synthesis of 6-bromo-2-hexanone using 1-methylcyclopentanol as starting material was as follows: a mixture of 1-methylcyclopentanol (4.00 g, 39.94 mmol) and potassium carbonate (K2CO3, 33.11 g, 239.6 mmol) in chloroform (CHCl3, 130 mL) was stirred for 15 min at 0 °C. Subsequently, bromine (10.23 mL, 199.7 mmol) was added slowly. The reaction mixture was continued to be stirred at 0°C for 2.5 hours. Upon completion of the reaction, the mixture was slowly poured into ice-cold saturated aqueous sodium thiosulfate (Na2S2O3, 100 mL). The organic layer was separated, washed with water (2 x 100 mL), dried over magnesium sulfate (MgSO4), filtered and concentrated in vacuum. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 3:1) to afford the target product 6-bromo-2-hexanone as a colorless oil (4 g) in 56% yield (98% purity, UV detection at 214 nm, no ESI signal detected). The 1H-NMR (400 MHz, CDCl3) data of the product were as follows: δ1.66-1.80 (m, 2H), 1.82-1.93 (m, 2H), 2.15 (s, 3H), 2.48 (t, J=7.3 Hz, 2H), 3.41 (t, J=6.5 Hz, 2H).

References[1] Journal of Organic Chemistry, 2000, vol. 65, # 18, p. 5831 - 5833
[2] Patent: US2018/244648, 2018, A1. Location in patent: Page/Page column 0289; 0290
[3] Russian Chemical Bulletin, 1999, vol. 48, # 11, p. 2080 - 2082
[4] Patent: WO2009/77990, 2009, A1. Location in patent: Page/Page column 63-64
[5] Patent: US2011/34516, 2011, A1. Location in patent: Page/Page column 34
1-Bromo-5-hexanone Preparation Products And Raw materials
Raw materialsPotassium carbonate-->Ethyl acetoacetate-->1-Bromo-3-chloropropane-->1-Methylcyclopentanol-->Chloroform
Preparation ProductsPROPENTOFYLLINE
Tag:1-Bromo-5-hexanone(10226-29-6) Related Product Information
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