296287
3,5-Dichlorobenzoyl chloride
96%
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About This Item
Fórmula lineal:
Cl2C6H3COCl
Número de CAS:
Peso molecular:
209.46
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
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.)
SMILES string
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 key
GGHLXLVPNZMBQR-UHFFFAOYSA-N
Application
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1C
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
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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Los clientes también vieron
Transformations of the herbicide N-(1, 1-dimethylpropynyl)-3, 5-dichlorobenzamide in soil.
Yih RY, et al.
Weed Sci., 604-607 (1970)
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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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