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(Dichloromethylene)dimethylammonium chloride

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(Dichloromethylene)dimethylammonium chloride Basic information

Product Name:
(Dichloromethylene)dimethylammonium chloride
Synonyms:
  • PHOSGENE IMINIUM CHLORIDE
  • PHOSGENIMINIUM CHLORIDE
  • (DICHLOROMETHYLENE)DIMETHYLAMMONIUM CHLORIDE
  • DICHLOROMETHYLENEDIMETHYLIMINIUM CHLORIDE
  • n,n-dimethylphosgeniminium chloride
  • VIEHE''SSALT
  • (Dichloromethylene)dimethylammonium chloride, Phosgeniminium chloride, Vilsmeier reagent
  • N,N-Dimethylphosgeniminium chloride~Phosgeniminium chloride~Viehes Salt
CAS:
33842-02-3
MF:
C3H6Cl2N.Cl
MW:
162.45
EINECS:
251-695-4
Product Categories:
  • Ammonium Chlorides (Quaternary)
  • Quaternary Ammonium Compounds
Mol File:
33842-02-3.mol
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(Dichloromethylene)dimethylammonium chloride Chemical Properties

Melting point:
183-187 °C (dec.) (lit.)
Boiling point:
267.81°C (rough estimate)
Density 
1.6902 (rough estimate)
refractive index 
1.6300 (estimate)
storage temp. 
2-8°C
solubility 
slightly sol. in Chloroform
form 
Crystalline Powder
color 
Light yellow
Water Solubility 
hydrolysis
Sensitive 
Moisture Sensitive
Merck 
14,9977
BRN 
4157987
CAS DataBase Reference
33842-02-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
14-34-37-29-22
Safety Statements 
26-36/37/39-45-8
RIDADR 
UN 3261 8/PG 3
WGK Germany 
3
3-10-21
HazardClass 
8
PackingGroup 
III
HS Code 
29252900

MSDS

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(Dichloromethylene)dimethylammonium chloride Usage And Synthesis

Chemical Properties

light yellow crystalline powder

Uses

Dichloromethylene-dimethyliminium Chloride is a useful chemical reagent. It has been used in the synthesis of 12-deoxychlorovulone II analogs via chloride nucleophilic substitution reaction catalyzed by Viehe''s salt.

Uses

Dichloromethylene-dimethyliminium chloride was used as reagent in the synthesis of selenourea and (R)-2-(2-chloroethyl)pyrrolidine-1-carboxylic acid ethyl ester. It was used for introducing amide chloride group into activated substrates.

Uses

Chlorinating agent; introduces amide chloride groups into activated substrates. Building block in organic synthesis.

General Description

Dichloromethylene-dimethyliminium chloride (Vilsmeier reagent) reacts with o-acetaminophenols under Meth-Cohn conditions to yield 2-formylpyrido[2,1-b]benzoxazoles.

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