3,5-DIMETHOXYBENZOYL CHLORIDE
3,5-DIMETHOXYBENZOYL CHLORIDE
  • CAS No.:17213-57-9
Other grades of this product :
3,5-DIMETHOXYBENZOYL CHLORIDE Basic information
Product Name:3,5-DIMETHOXYBENZOYL CHLORIDE
Synonyms:3,5-DIMETHOXYBENZOYL CHLORIDE;AKOS 91393;LABOTEST-BB LTBB000778;TIMTEC-BB SBB009969;Benzoyl chloride, 3,5-dimethoxy-;3,5-Dimethoxybenzoyl chloride, ca. 92%;3,5-Dimethoxybenzoic acid chloride;3,5-Dimethoxybenzoyl chloride 97%
CAS:17213-57-9
MF:C9H9ClO3
MW:200.62
EINECS:241-256-5
Product Categories:Aromatic Halides (substituted);Building Blocks for Dendrimers;Functional Materials;Acid Halides;Carbonyl Compounds;Organic Building Blocks
Mol File:17213-57-9.mol
3,5-DIMETHOXYBENZOYL CHLORIDE Chemical Properties
Melting point 43-46 °C (lit.)
Boiling point 157-158 °C/16 mmHg (lit.)
density 1.2799 (rough estimate)
refractive index 1.5230 (estimate)
Fp >230 °F
form powder to lump
color White to Light yellow
Water Solubility It hydrolyzes in water.
Sensitive Moisture Sensitive
BRN 511839
CAS DataBase Reference17213-57-9(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
10-19-21
HazardClass 8
PackingGroup II
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
3,5-DIMETHOXYBENZOYL CHLORIDE Usage And Synthesis
Chemical Propertiesoff-white to light brown crystalline powder
Uses3,5-Dimethoxybenzoyl chloride was used to study the mechanism and kinetics of solvolysis of 3,4- and 3,5-dimethoxybenzoyl chlorides in various binary solvents. 3,5-Dimethoxybenzoyl chloride undergoes addition reaction with 4,4-dimethyl-2-pentyne in presence of AlCl3 via 1,2- methyl shift. It is used as a chemical and organic intermediate.
Uses3,5-Dimethoxybenzoyl chloride was used to study the mechanism and kinetics of solvolysis of 3,4- and 3,5-dimethoxybenzoyl chlorides in various binary solvents.
General Description3,5-Dimethoxybenzoyl chloride undergoes addition reaction with 4,4-dimethyl-2-pentyne in presence of AlCl3 via 1,2- methyl shift.

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