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Sigma-Aldrich

3,5-二氯苯甲酰氯

96%

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About This Item

线性分子式:
Cl2C6H3COCl
CAS号:
2905-62-6
分子量:
209.46
EC號碼:
220-813-6
MDL號碼:
MFCD00009817
分類程式碼代碼:
12352100
PubChem物質ID:
24857848
NACRES:
NA.22

蒸汽壓力

0.1 mmHg ( 32 °C)

化驗

96%

形狀

solid

折射率

n20/D 1.582 (lit.)

bp

135-137 °C/25 mmHg (lit.)

mp

28 °C (lit.)

SMILES 字串

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

InChI

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

InChI 密鑰

GGHLXLVPNZMBQR-UHFFFAOYSA-N

應用

3,5-Dichlorobenzoyl chloride has been used in the preparation of:
  • N-(1,1-dimethylpropynyl)-3,5-dichlorobenzamide, herbicide
  • (3,5-dichlorophenyl)(2-(4-methoxyphenyl)-5-methylbenzofuran-3-yl)methanone

象形圖

CorrosionExclamation mark
GHS05,GHS07

訊號詞

Danger

危險聲明

H302,H314

危險分類

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

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

235.4 °F - closed cup

閃點（°C）

113 °C - closed cup

個人防護裝備

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)
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
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
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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