77460
2-Chloroacetophenone
purum, ≥98.0% (GC)
동의어(들):
ω-Chloroacetophenone, Phenacyl chloride
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5COCH2Cl
CAS 번호:
Molecular Weight:
154.59
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-531-1
Beilstein/REAXYS Number:
507950
MDL number:
Assay:
≥98.0% (GC)
Form:
crystals
InChI key
IMACFCSSMIZSPP-UHFFFAOYSA-N
InChI
1S/C8H7ClO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2
SMILES string
ClCC(=O)c1ccccc1
grade
purum
assay
≥98.0% (GC)
form
crystals
bp
244-245 °C (lit.)
mp
53-56 °C, 54-56 °C (lit.)
density
1.324 g/mL at 25 °C (lit.)
functional group
chloro, ketone, phenyl
Quality Level
Gene Information
human ... PTPN6(5777)
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General description
2-Chloroacetophenone is an organic building block used in the synthesis of heterocyclic compounds. It has low solubility in water but can be soluble in alcohols, ethers and other organic solvents.
Application
2-Chloroacetophenone can be used in the synthesis of phenyl acetic acid by Photo-Favorskii rearrangement. It is also used in the preparation of 1-(2-chlorophenyl)ethanol via asymmetric hydrogenation reaction.
signalword
Danger
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
저장 등급
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Expanding the [1,2]-aryl migration to the synthesis of substituted indoles.
Tao Pei et al.
Angewandte Chemie (International ed. in English), 47(22), 4231-4233 (2008-04-30)
Wladimir Solodenko et al.
Molecular diversity, 9(4), 333-339 (2005-11-29)
The preparation of a new palladium(II) complex with a 2-pyridinealdoxime ligand and its use as a Pd(0) precatalyst in the cross-coupling Suzuki-Miyaura reaction is described. Several concepts for the immobilization of this catalytic system are presented and compared in order
Yan Xie et al.
Bioresource technology, 101(3), 1054-1059 (2009-09-22)
Target reaction-oriented screening from soil samples yielded a ketone reductase-producing Bacillus sp., strain ECU0013, which exhibits excellent stereoselectivity, high substrate tolerance and is capable of regenerating the required cofactor with glucose as a co-substrate. Whole-cells catalyzed the asymmetric reduction of
Qing Xie et al.
Biotechnology progress, 22(5), 1301-1304 (2006-10-07)
The asymmetric reduction of o-chloroacetophenone 1 with Candida pseudotropicalis 104 produced the corresponding (S)-1-(2-chloro-phenyl)-ethanol 2 with the enantiomeric excess (ee >99%) without addition of any cosolvent. The cell could tolerate high ketone 1 concentration of 233.8 mmol/L (i.e., 36 g/L)
Gregg M Recer et al.
Regulatory toxicology and pharmacology : RTP, 36(1), 1-11 (2002-10-18)
In 1996, the New York State Department of Health was charged by the State Legislature to develop regulations regarding the types of self-defense spray devices which could lawfully be purchased, possessed, and used in New York State. Prior to this
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