10904
3-Chloro-2-butanone
Wacker Chemie AG, ≥96.0% (GC)
Synonym(s):
Chloro-MEK
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1 KG
$299.00
25 KG
$2,250.00
About This Item
Linear Formula:
CH3CHClCOCH3
CAS Number:
Molecular Weight:
106.55
Beilstein:
385637
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥96.0% (GC)
manufacturer/tradename
Wacker Chemie AG
refractive index
n20/D 1.421 (lit.)
bp
114-117 °C (lit.)
density
1.055 g/mL at 25 °C (lit.)
SMILES string
CC(Cl)C(C)=O
InChI
1S/C4H7ClO/c1-3(5)4(2)6/h3H,1-2H3
InChI key
OIMRLHCSLQUXLL-UHFFFAOYSA-N
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General description
3-Chloro-2-butanone when treated with aq. sodium thiocyanate forms 3-thiocyano-2-butanone[1].
Application
3-Chloro-2-butanone was used to study various carbonylic compounds as substrates for 4-hydroxyacetophenone monooxygenase from Pseudomonas fluorescens ACB[2].
Other Notes
prices for bulk quantities on request
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
82.4 °F - closed cup
Flash Point(C)
28 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Reactions of 3-Thiocyano-2-butanone. I. The Preparation of 2-Substituted-4, 5-dimethylthiazoles.
Gregory JT and Mathes RA.
Journal of the American Chemical Society, 74(7), 1719-1720 (1952)
Nanne M Kamerbeek et al.
Applied and environmental microbiology, 69(1), 419-426 (2003-01-07)
The 4-hydroxyacetophenone monooxygenase (HAPMO) from Pseudomonas fluorescens ACB catalyzes NADPH- and oxygen-dependent Baeyer-Villiger oxidation of 4-hydroxyacetophenone to the corresponding acetate ester. Using the purified enzyme from recombinant Escherichia coli, we found that a broad range of carbonylic compounds that are
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