2-Chloro-1,3-dimethylimidazolidinium chloride
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
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)
MSDS
- Language:English Provider:SigmaAldrich
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
- https://www.sigmaaldrich.com/catalog/product/aldrich/529249?lang=en®ion=US
- https://pubs.acs.org/doi/abs/10.1021/jo990210y
- www.sciencedirect.com/science/article/pii/S004040391001395X
- 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.
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2-Chloro-1,3-dimethylimidazolidinium chloride(37091-73-9)Related Product Information
- Ammonium chloride
- 1,3-Dimethyl-2-imidazolidinone
- Sodium chloride
- Epichlorohydrin
- DIMETHYLALUMINUM CHLORIDE
- DIMETHYLTIN DICHLORIDE
- Polyvinyl chloride
- Imidazolidine
- Choline chloride
- Calcium chloride
- Methylene Chloride
- Difluorochloromethane
- Chloroacetic acid
- 2-Chloro-1H-imidazole
- CHLOROFORMAMIDINE HYDROCHLORIDE
- (Chloromethylene)dimethyliminium chloride
- (4S,5S)-2-CHLORO-1,3-DIMETHYL-4,5-DIPHENYL-1-IMIDAZOLINIUM CHLORIDE
- (DIMETHYLAMINOMETHYLENE)DIMETHYLAMMONIUM CHLORIDE