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2,4,6-Trichlorobenzoyl chloride

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2,4,6-Trichlorobenzoyl chloride Basic information

Product Name:
2,4,6-Trichlorobenzoyl chloride
Synonyms:
  • 2,4,6-TRICHLOROBENZOYL CHLORIDE
  • 2,4,6-TRICHLORBENZOYLCHLORID
  • 2,4,6-TRICHLOROBENZOYL CHLORIDE 98%
  • 2,4,6-TrichlorobenzoyChloride
  • 2,4,6-Trichlorobenzoic acid chloride
  • 2,4,6-Trichlorobenzoyl chloride,98%
  • 2,4,6-Ttrichlorobenzoyl chloride
  • 2,4,6-Trichlorobenzoyl chloride, 98% 5GR
CAS:
4136-95-2
MF:
C7H2Cl4O
MW:
243.9
Product Categories:
  • Condensation & Active Esterification
  • Synthetic Organic Chemistry
  • Acid Halides
  • Carbonyl Compounds
  • Organic Building Blocks
Mol File:
4136-95-2.mol
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2,4,6-Trichlorobenzoyl chloride Chemical Properties

Melting point:
165-166 °C
Boiling point:
107-108 °C/6 mmHg (lit.)
Density 
1.561 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5754(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Acetonitrile (Slightly), Chloroform (Sparingly), Ethyl Acetate (Slightly)
form 
Liquid
Specific Gravity
1.561
color 
Clear yellow
Water Solubility 
Reacts with water.
Sensitive 
Moisture Sensitive
BRN 
2050280
InChIKey
OZGSEIVTQLXWRO-UHFFFAOYSA-N
CAS DataBase Reference
4136-95-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-27-28-36/37/39-45-25
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
HazardClass 
8
PackingGroup 
II
HS Code 
29163990

MSDS

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2,4,6-Trichlorobenzoyl chloride Usage And Synthesis

Description

2,4,6-Trichlorobenzoyl chloride is a chemical compound that forms during the synthesis of benzalkonium chloride. It can be used as an efficient method for the synthesis of fatty acids and cyclic peptides. The reaction products are chlorinated and have a hydroxyl group. It is used in the synthesis of fatty acids by reacting with acetic acid to produce a chlorinated fatty acid. Hydroxyl groups react with 2,4,6-trichlorobenzoyl chloride to form a chlorinated hydroxy fatty acid.

Chemical Properties

clear yellow liquid

Uses

2,4,6-Trichlorobenzoyl chloride may be used in the preparation of:

  • γ-lactone and δ-lactone
  • aliphatic aromatic anhydrides, required for the synthesis of amphiphilic hyaluronan
  • mixed anhydride, required for the synthesis of angelate esters
  • synthesis of both spongistatin 1 and spongistatin 2
  • large-ring lactones in high yields.

Application

2,4,6-Trichlorobenzoyl chloride has been shown to inhibit cervical cancer cell growth and reduce the incidence of cervical cancer by inhibiting DNA replication.

2,4,6-Trichlorobenzoyl chlorideSupplier

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