Basic information Description Sources Safety Supplier Related

2-Chloro-1,3-dimethylimidazolidinium chloride

Basic information Description Sources Safety Supplier Related

2-Chloro-1,3-dimethylimidazolidinium chloride Basic information

Product Name:
2-Chloro-1,3-dimethylimidazolidinium chloride
Synonyms:
  • 1,3-DIMETHYL-2-CHLOROIMIDAZOLINIUM CHLORIDE
  • 2-CHLORO-1,3-DIMETHYLIMIDAZOLIDINIUM CHLORIDE
  • 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLORIDE
  • Chlorodimethyllimidazoliniumchloride
  • 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLOR
  • 2-CHLORO-1,3-DIMETHYLIMIDAZOLIUM CHLORIDE
  • 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLORIDE: (CA. 25% IN DICHLOROMETHANE)
  • 2-CHLORO-1,3-DIMETHYLIMIDAZOLINIUM CHLORIDE 98+%
CAS:
37091-73-9
MF:
C5H10Cl2N2
MW:
169.05
EINECS:
629-540-0
Product Categories:
  • Amines
  • Heterocycles
  • Biochemistry
  • Condensation & Active Esterification
  • Coupling Reactions (Peptide Synthesis)
  • Peptide Synthesis
  • Synthetic Organic Chemistry
  • Phosphonium/Uronium/Formamidinium
  • Phosphonium/Uronium/FormamidiniumSynthetic Reagents
  • Coupling
  • Peptide Synthesis
Mol File:
37091-73-9.mol
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2-Chloro-1,3-dimethylimidazolidinium chloride Chemical Properties

Melting point:
133-140 °C (lit.)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Chloroform, Methanol, Water
form 
Powder or Crystalline Powder
color 
White to off-white
Merck 
13,3424
Stability:
Hygroscopic
InChIKey
AEBBXVHGVADBHA-UHFFFAOYSA-M
CAS DataBase Reference
37091-73-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
1593
WGK Germany 
3
3-10-21
HazardClass 
6.1
PackingGroup 
III
HS Code 
29332900

MSDS

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2-Chloro-1,3-dimethylimidazolidinium chloride Usage And Synthesis

Description

2-Chloro-1,3-dimethylimidazolidinium chloride has various applications including being used as activating agent in total synthesis of macroviracin A, cycloviracin B1 and cyclic silanes; used as reagent for synthesis of tagged glucose as an intermediate in the synthesis of branched oligosaccharides; used as fluorescent chemosensors; 1,2-Diamines as inhibitors of co-activator associated arginine methyltransferase 1; used as allosteric glucokinase activators; as reactant for synthesis of organic azides from primary amines and for aza-Henry reactions1. It can act as a powerful dehydrating agent, replacing DCC under nearly neutral conditions, and has application for the construction of heterocycles2. Moreover, it can be used for one-pot synthesis of 2-aminobenzimidazoles3. It is also applicable to chlorination, oxidation, reduction, and rearrangement under nearly neutral conditions4.

Sources

  1. https://www.sigmaaldrich.com/catalog/product/aldrich/529249?lang=en&region=US
  2. https://pubs.acs.org/doi/abs/10.1021/jo990210y
  3. www.sciencedirect.com/science/article/pii/S004040391001395X
  4. J. Org. Chem., 1999, 64 (16), pp 5832–5835

Chemical Properties

Brown Solid

Uses

Reagent for synthesis of:
Tagged glucose as an intermediate in the synthesis of branched oligosaccharides
Fluorescent chemosensors
1,2-Diamines as inhibitors of co-activator associated arginine methyltransferase 1
Allosteric glucokinase activators

Reactant for synthesis of:
Organic azides from primary amines

Reagent for aza-Henry reactions

Uses

Used in the one-pot synthesis of 2-aminobenzimidazoles.

2-Chloro-1,3-dimethylimidazolidinium chlorideSupplier

Suzhou Highfine Biotech Co., Ltd Gold
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021-61259108 18621169109
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