추천 제품
Grade
produced by Wacker Chemie AG, Burghausen, Germany
분석
≥96.0% (GC)
포함
~0.1% Drapex 39 as stabilizer
refractive index
n20/D 1.432 (lit.)
bp
120 °C (lit.)
solubility
H2O: soluble 10 parts
alcohol: miscible
chloroform: miscible
diethyl ether: miscible
density
1.162 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
CC(=O)CCl
InChI
1S/C3H5ClO/c1-3(5)2-4/h2H2,1H3
InChI key
BULLHNJGPPOUOX-UHFFFAOYSA-N
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일반 설명
Chloroacetone undergoes direct aldol reaction with 4-nitrobenzaldehyde catalyzed by L-proline amides. It reacts with carboxylic acids to form ester derivatives.
애플리케이션
Chloroacetone was used in microbial asymmetric reduction of chloracetone to synthesize chiral 1,2-epoxy propane. It was used in analysis of acids by gas chromatography. It was also used in the syntheis of methylthiazole derivatives by reacting with 1-((3-(naphtho[2,1-b]furan-2-yl)-1-phenyl-1H-pyrazol-4-yl) methylene)-2-phenylhydrazone.
기타 정보
prices for bulk quantities on request
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
95.0 °F - closed cup
Flash Point (°C)
35 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Analysis of carboxylic acids by gas chromatography. Derivatisation using chloroacetone.
Chromatographia, 18(6), 309-312 (1984)
Synthesis of optically pure 1, 2-epoxypropane by microbial asymmetric reduction of chloroacetone.
Applied Microbiology and Biotechnology, 38(3), 297-300 (1992)
Molecules (Basel, Switzerland), 16(1), 307-318 (2011-01-27)
Vilsmeier formylation of 2-(1-phenylhydrazonoethyl)naphtho[2,1-b]furan (2) gave 3-naphtho[2,1-b]furan-2-yl-1-phenyl-1H-pyrazole-4-carbaldehyde (3), which was reacted with C- and N-nucleophiles to afford naphthofuranpyrazol derivatives 4-8. Treatment of 2-[(3-(naphtho[2,1-b]furan-2-yl)-1-phenyl-1H-pyrazol-4-yl)methylene]-malononitrile (4a) with reactants having active hydrogen and Et₃N gave the corresponding pyrazoline, pyran and chromene addition product
L-Proline amide-catalyzed direct asymmetric aldol reaction of aldehydes with chloroacetone.
Tetrahedron, 62(2), 346-351 (2006)
Dose-response relationships for mutations induced in E. coli by some model compounds. With an addendum: Reaction kinetics in water of chloroethylene oxide, chloroacetaldehyde, and chloroacetone.
Hereditas, 101(1), 57-68 (1984-01-01)
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