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C19686

2-Chloroacetophenone

Name: 2-Chloroacetophenone
Brand: ALDRICH

98%

Synonym(s):

ω-Chloroacetophenone, Phenacyl chloride

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About This Item

Linear Formula:

C₆H₅COCH₂Cl

CAS Number:

532-27-4

Molecular Weight:

154.59

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892454

EC Number:

208-531-1

Beilstein/REAXYS Number:

507950

MDL number:

MFCD00000933

Assay:

98%

Form:

crystals

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Properties

Quality Level

200

assay

98%

form

crystals

bp

244-245 °C (lit.)

mp

54-56 °C (lit.)

density

1.324 g/mL at 25 °C (lit.)

SMILES string

ClCC(=O)c1ccccc1

InChI

1S/C8H7ClO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2

InChI key

IMACFCSSMIZSPP-UHFFFAOYSA-N

Gene Information

human ... PTPN6(5777)

Description

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pictograms

GHS06,GHS08,GHS05

signalword

Danger

hcodes

H300,H311 + H331,H315,H318,H334,H335

pcodes

P261 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 - P305 + P351 + P338

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

Storage Class

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

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2-Pyridinealdoxime, a new ligand for a Pd-precatalyst: application in solid-phase-assisted Suzuki-Miyaura reaction.

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

Thermal decomposition studies of riot control agent ω-chloroacetophenone (CN) by pyrolysis-gas chromatography-mass spectrometry.

Anil K Nigam et al.

Journal of hazardous materials, 184(1-3), 506-514 (2010-09-17)

Pyrolysis-GC/MS system with on-line micro-furnace was used to make rapid evaluation of ω-chloroacetophenone (CN) decomposition under inert thermal atmospheres. The volatile products evolved during pyrolysis were analyzed by thermal gravimetric analysis (TGA) and Py-GC/MS to obtain specific thermogram and pyrogram.

Asymmetric reduction of o-chloroacetophenone with Candida pseudotropicalis 104.

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)

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Global Trade Item Number

SKU	GTIN
C19686-100G	04061833474884
C19686-500G	04061831835250