77460
2-Chloroacetophenone
purum, ≥98.0% (GC)
别名:
ω-Chloroacetophenone, Phenacyl chloride
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关于此项目
线性分子式:
C6H5COCH2Cl
化学文摘社编号:
分子量:
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
产品名称
2-Chloroacetophenone, purum, ≥98.0% (GC)
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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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.
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.
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
存储类别
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
法规信息
危险化学品
此项目有
Preparation of microgel-supported chiral catalysts and their application in the asymmetric hydrogenation of aromatic ketones
Deng J, et al.
Reactive and Functional Polymers, 72, 378-382 (2012)
Experimental study of the adsorption of 2-Chloroacetophenone at the air-environmental water interface
Hao, et al.
Frontiers in environmental science., 10, 2254-2254 (2022)
Ionic liquid mediated and promoted one-pot green synthesis of new isoxazolyl dihydro-1 H-indol-4 (5 H)-one derivatives at ambient temperature
Modugu, et al.
Cogent Chemistry , 3, 1318693-1318693 (2017)
Principles of coaxial illumination for photochemical reactions: Part 2. Model validation
Meir, et al.
Journal of advanced materials and processing, 2 (2020)
Lenilson C Rocha et al.
Biotechnology letters, 31(10), 1559-1563 (2009-06-06)
The asymmetric reduction of 2-chloro-1-phenylethanone (1) by seven strains of marine fungi was evaluated and afforded (S)-(-)-2-chloro-1-phenylethanol with, in the best case, an enantiomeric excess of 50% and an isolated yield of 60%. The ability of marine fungi to catalyse
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