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Merck
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주요 문서

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C19708

Sigma-Aldrich

4′-Chloroacetophenone

97%

동의어(들):

1-(4-Chlorophenyl)-1-ethanone, 1-(p-Chlorophenyl)ethanone, 1-Acetyl-4-chlorobenzene, 4-Acetyl-1-chlorobenzene

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모든 사진(2)

About This Item

Linear Formula:
ClC6H4COCH3
CAS Number:
99-91-2
Molecular Weight:
154.59
Beilstein:
386014
EC Number:
202-800-7
MDL number:
MFCD00000624
UNSPSC 코드:
12352100
PubChem Substance ID:
24892455
NACRES:
NA.22

vapor pressure

8 mmHg ( 90 °C)

Quality Level

100

분석

97%

양식

liquid

refractive index

n20/D 1.554 (lit.)

bp

232 °C (lit.)

mp

14-18 °C (lit.)

density

1.192 g/mL at 25 °C (lit.)

SMILES string

CC(=O)c1ccc(Cl)cc1

InChI

1S/C8H7ClO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

InChI key

BUZYGTVTZYSBCU-UHFFFAOYSA-N

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관련 카테고리

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H302,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

Flash Point (°F)

194.0 °F - closed cup

Flash Point (°C)

90 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
STBH7632
S63208V
S63208
01220PH
05621KH

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

J Havel et al.
Applied and environmental microbiology, 59(8), 2706-2712 (1993-08-01)
A defined mixed culture, consisting of an Arthrobacter sp. and a Micrococcus sp. and able to grow with 4-chloroacetophenone as a sole source of carbon and energy, was isolated. 4-Chlorophenyl acetate, 4-chlorophenol, and 4-chlorocatechol were identified as metabolites through comparison
Lidiane S Araújo et al.
Marine drugs, 9(5), 889-905 (2011-06-16)
Several microorganisms were isolated from soil/sediment samples of Antarctic Peninsula. The enrichment technique using (RS)-1-(phenyl)ethanol as a carbon source allowed us to isolate 232 psychrophile/psychrotroph microorganisms. We also evaluated the enzyme activity (oxidoreductases) for enantioselective oxidation reactions, by using derivatives
F Pfannkuch et al.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 218(4), 177-184 (1982-01-01)
Solutions of various concentrations of chloracetophenone (dissolved in 1, 1, 1, trichlorethane) were trickled on the corneas of rabbits. The substance was either applied to the center or to the limbus, or simultaneously to the center and limbus of the
Xiao-Hong Chen et al.
BMC biotechnology, 11, 110-110 (2011-11-22)
Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds. The recently isolated strain Acetobacter sp. CCTCC M209061 showed exclusive
Daniel I Perez et al.
Bioorganic & medicinal chemistry, 17(19), 6914-6925 (2009-09-15)
Thienylhalomethylketones, whose chemical, biological, and pharmaceutical data are here reported, are the first irreversible inhibitors of GSK-3beta described to date. Their inhibitory activity is likely related to the cysteine residue present in the ATP-binding site, which is proposed as a

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