Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Acyl halide >  2,4,6-Trichlorobenzoyl chloride

2,4,6-Trichlorobenzoyl chloride

Basic information Safety Supplier Related

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
More
Less

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)
More
Less

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

More
Less

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

Suzhou Highfine Biotech Co., Ltd Gold
Tel
0512-68311833 13962195826
Email
wuhao@highfine.com
Chemsigma International Co.,Ltd Gold
Tel
+86-19951791336 18951874645
Email
shijiao.wu@chemsigma.com
Shandong Winner Biotechnology Co., Ltd. Gold
Tel
15315319889 15315319889
Email
wannaswsw@163.com
Nanyang Runhong Pharmaceutical Technology Co., Ltd Gold
Tel
17637776888
Email
17637776888@163.com
Hebei Boxin Biotechnology Co. , Ltd. Gold
Tel
19131160546
Email
2681315246@qq.com