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Postion:Product Catalog >Chemical Reagents>Organic reagents>Acyl halide>3,5-Dichlorobenzoyl chloride
3,5-Dichlorobenzoyl chloride
  • 3,5-Dichlorobenzoyl chloride
  • 3,5-Dichlorobenzoyl chloride
  • 3,5-Dichlorobenzoyl chloride
  • 3,5-Dichlorobenzoyl chloride
  • 3,5-Dichlorobenzoyl chloride

3,5-Dichlorobenzoyl chloride NEW

Price Get Latest Price
Package 25KG
Min. Order: 1KG
Supply Ability: 50000KG/month
Update Time: 2023-10-10

Product Details

Product Name: 3,5-Dichlorobenzoyl chloride CAS No.: 2905-62-6
EC-No.: 220-813-6 Min. Order: 1KG
Purity: 99% Supply Ability: 50000KG/month
Release date: 2023/10/10

CAS:2905-62-6
MF:C7H3Cl3O
MW:209.46
EINECS:220-813-6
Product Categories:Acid Halides;Building Blocks;ACIDHALIDE;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Acid Halides;Carbonyl Compounds;Organic Building Blocks
Mol File:2905-62-6.mol
Article illustration

3,5-Dichlorobenzoyl chloride Chemical Properties
Melting point 28 °C (lit.)
Boiling point 135-137 °C/25 mmHg (lit.)
density 135
vapor pressure 0.1 mm Hg ( 32 °C)
refractive index n20/D 1.582(lit.)
Fp >230 °F
storage temp. Refrigerator (+4°C)
solubility soluble in Benzene,Toluene
form powder to lump to clear liquid
color White or Colorless to Almost white or Almost colorless
Sensitive Moisture Sensitive
BRN 1940681
InChIKeyGGHLXLVPNZMBQR-UHFFFAOYSA-N
LogP3.32
CAS DataBase Reference2905-62-6(CAS DataBase Reference)
NIST Chemistry Reference3,5-Dichlorobenzoyl chloride(2905-62-6)
EPA Substance Registry SystemBenzoyl chloride, 3,5-dichloro- (2905-62-6)
3,5-Dichlorobenzoyl chloride Usage And Synthesis
Chemical Propertiesclear colorless to light yellow liquid or low
Uses3,5-Dichlorobenzoyl chloride is a useful intermediate for organic synthesis and other pharmaceutical processes.
Uses3,5-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

Flammability and ExplosibilityNon flammable
Synthesis3,5-Dichlorobenzoyl chloride is obtained by reacting by aryl carboxylic acid with DMF.Dissolve aryl carboxylic acid (10.0 mmol) in 50 mL DCM with drops of DMF to a 100 mL roundbottomed flask. Cool the mixture to 0°C. Add oxalyl chloride (20.0 mmol, 2.0 equivalents) dropwise to the reaction mixture. Allow the reaction mixture to react for another 4 hours. Concentrate the solvent in vacuo. Use the remaining residue directly.
Article illustrationFig The synthetic method of Article illustration3,5-Dichlorobenzoyl chloride

Packing &shipping&Payment

Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
Quantity(Kilograms)1 - 10000>10000
Est. Time(days)5To be negotiated

Article illustration

Article illustrationCompany information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.

Article illustrationAdvantage
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Article illustration






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