1,3,5-Benzenetricarboxylic acid chloride

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+%;1,3,5-Benzene;1,3,5-BENZENETRICARBOXYLICACIDTRICHLORIDE;Benzene-1,3,5-tricarbonyl chloride, Trimesic acid trichloride, Trimesoyl chloride;1,3,5-Tris(chlorocarbonyl)benzene
CAS:4422-95-1
MF:C9H3Cl3O3
MW:265.48
EINECS:224-594-8
Product Categories:bc0001
Mol File:4422-95-1.mol
1,3,5-Benzenetricarboxylic acid chloride Structure
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
Fp >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 Reference4422-95-1(CAS DataBase Reference)
NIST Chemistry Reference1,3,5-Benzenetricarbonyl trichloride(4422-95-1)
EPA Substance Registry System1,3,5-Benzenetricarbonyl trichloride (4422-95-1)
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 Information
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1,3,5-Benzenetricarboxylic acid chloride Usage And Synthesis
Chemical Propertiesclear yellow liquid after melting
Uses1,3,5-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.
Uses1,3,5-Benzenetricarbonyl chloride 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.
UsesSpecialty organic.
General Description1,3,5-Benzenetricarbonyl trichloride reacts with propargyl alcohol to yield triprop-2-ynyl benzene-1,3,5-tricarboxylate.
Benzyl chloride 4-Nitrobenzoyl chloride 3-Methylbenzyl chloride 5-METHYLISOPHTHALALDEHYDE m-Phthalaldehyde 3-(Chloromethyl)benzoyl chloride 3-Methylbenzoyl chloride Terephthaloyl chloride 1,3,5-Benzenetricarboxaldehyde Ammonium chloride 4-Nitrobenzenesulfonyl chloride 1,3-Bis(chloromethyl)benzene 3,5-Dimethylbenzaldehyde Benzoyl chloride Potassium chloride Thionyl chloride 2-​[[(2-​ethylphenyl)​(2-​hydroxyethyl)​amino]​methyl]​-​3,​3-​difluoro-Propanenitrile EPA

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