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1,3,5-Benzenetricarboxylic acid chloride

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1,3,5-Benzenetricarboxylic acid chloride Basic information

Product Name:
1,3,5-Benzenetricarboxylic acid chloride
Synonyms:
  • 1,3,5-BENZENETRICARBONYL TRICHLORIDE, 98
  • 1,3,5-Bnezenetricarbonyltrichloride
  • 1,3,5-Trichlorobenzoylchloride
  • 1,3,5-Benzenetricarbonylchloride,98+%
  • Trimesoyl trichloride
  • 1,3,5-Benzene
  • 1,3,5-BENZENETRICARBOXYLICACIDTRICHLORIDE
  • Benzene-1,3,5-tricarbonyl chloride, Trimesic acid trichloride, Trimesoyl chloride
CAS:
4422-95-1
MF:
C9H3Cl3O3
MW:
265.48
EINECS:
224-594-8
Product Categories:
  • bc0001
Mol File:
4422-95-1.mol
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1,3,5-Benzenetricarboxylic acid chloride Chemical Properties

Melting point:
32-38 °C (lit.)
Boiling point:
180 °C/16 mmHg (lit.)
Density 
1.487 g/mL at 25 °C (lit.)
refractive index 
1.5945-1.5965
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
decomposes
form 
Liquid
color 
Clear colorless to slightly yellow
Water Solubility 
decomposes
Sensitive 
Moisture Sensitive
BRN 
2940936
CAS DataBase Reference
4422-95-1(CAS DataBase Reference)
NIST Chemistry Reference
1,3,5-Benzenetricarbonyl trichloride(4422-95-1)
EPA Substance Registry System
1,3,5-Benzenetricarbonyl trichloride (4422-95-1)
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Safety Information

Hazard Codes 
C
Risk Statements 
14-22-34
Safety Statements 
26-36/37/39-45-24/25
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
10-19
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29173980

MSDS

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1,3,5-Benzenetricarboxylic acid chloride Usage And Synthesis

Chemical Properties

clear yellow liquid after melting

Uses

Specialty organic.

Uses

1,3,5-Benzenetricarbonyl trichloride was used in the synthesis of chiral azoaromatic dendrimeric systems. It was used to study the structure of activated composite membranes containing organophosphorus extractants as carriers. It was the starting material for two tritopic amides derived from 3- and 4-methylaminopyridine which self-assembled into nanoballs on treatment with palladium(II) nitrate in DMSO.

General Description

1,3,5-Benzenetricarbonyl trichloride reacts with propargyl alcohol to yield triprop-2-ynyl benzene-1,3,5-tricarboxylate.

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