3,5-Dichlorobenzoyl chloride

Name: 3,5-Dichlorobenzoyl chloride
Brand: ALDRICH

96%

Slide 1 of 2

About This Item

Linear Formula:

Cl₂C₆H₃COCl

CAS Number:

2905-62-6

Molecular Weight:

209.46

NACRES:

NA.22

PubChem Substance ID:

24857848

UNSPSC Code:

12352100

EC Number:

220-813-6

MDL number:

MFCD00009817

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Key Documents

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Product Name

3,5-Dichlorobenzoyl chloride, 96%

InChI key

GGHLXLVPNZMBQR-UHFFFAOYSA-N

InChI

1S/C7H3Cl3O/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3H

SMILES string

ClC(=O)c1cc(Cl)cc(Cl)c1

vapor pressure

0.1 mmHg ( 32 °C)

assay

96%

form

solid

refractive index

n20/D 1.582 (lit.)

bp

135-137 °C/25 mmHg (lit.)

mp

28 °C (lit.)

Application

3,5-Dichlorobenzoyl chloride has been used in the preparation of:

N-(1,1-dimethylpropynyl)-3,5-dichlorobenzamide, herbicide[1]
(3,5-dichlorophenyl)(2-(4-methoxyphenyl)-5-methylbenzofuran-3-yl)methanone[2]

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H302,H314

pcodes

P260 - P270 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Transformations of the herbicide N-(1, 1-dimethylpropynyl)-3, 5-dichlorobenzamide in soil.

Yih RY, et al.

Weed Sci., 604-607 (1970)

Preparation of an O-[2-(methacryloyloxy)-ethylcarbamoyl]-10,11-dihydroquinidine-silica hybrid monolithic column for the enantioseparation of amino acids by nano-liquid chromatography.

Dongsheng Xu et al.

Journal of chromatography. A, 1593, 63-72 (2019-02-05)

An O-[2-(methacryloyloxy)-ethylcarbamoyl]-10,11-dihydroquinidine (MQD)-silica hybrid monolithic column was prepared by a facile "one-step" strategy within a 100 μm I.D. capillary. The influence of the methanol, ethylene glycol and water volume ratio, reaction temperature and time, cetyltrimethylammonium bromide and MQD monomers content

Synthesis and antimicrobial evaluation of new benzofuran derivatives.

Xizhen Jiang et al.

European journal of medicinal chemistry, 46(8), 3526-3530 (2011-05-17)

Thirteen compounds, based on benzofuran skeleton bearing aryl substituents at its C-3 position through methanone linker, were synthesized and screened for their antibacterial and antifungal activities against four bacteria Escherichia coli, Staphylococcus aureus, Methicillin-resistant S.aureus, Bacillus subtilis, and a fungus

Synthetic Approaches for Poly(Phenylene) Block Copolymers via Nickel Coupling Reaction for Fuel Cell Applications.

Adam F Nugraha et al.

Polymers, 12(7) (2020-07-24)

Several methods to synthesize poly(phenylene) block copolymers through the nickel coupling reaction were attempted to reduce the use of expensive nickel catalysts in polymerization. The model reaction for poly(phenylene) having different types of dichlorobenzene derivative monomers illustrated the potential use

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