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| (Chloromethylene)dimethyliminium chloride Basic information |
| Product Name: | (Chloromethylene)dimethyliminium chloride | | Synonyms: | N-CHLOROMETHYLEN-N,N-DIMETHYLAMMONIUM CHLORIDE;VILSMEIER REAGENT;(CHLOROMETHYLENE)DIMETHYLAMMONIUM CHLORIDE;CHLOROMETHYLENEDIMETHYLIMINIUM CHLORIDE;n-(chloromethylene)-n-methyl-methanaminiuchloride;Vilsmeier;N-Chloromethylene-N,N-Dimethyl Ammonium Chloride;(Chloromethylene)dimethylammoniumchlorlde | | CAS: | 3724-43-4 | | MF: | C3H7ClN.Cl | | MW: | 128 | | EINECS: | 425-970-6 | | Product Categories: | | Mol File: | 3724-43-4.mol |
| (Chloromethylene)dimethyliminium chloride Chemical Properties |
| (Chloromethylene)dimethyliminium chloride Usage And Synthesis |
| Chemical Properties | Pale brown to yellowish-brown crystalline powder | | Uses | (Chloromethylene)dimethylammonium chloride is used in the synthesis of beta-lactams, n-vinyl substituted indoles and fused 2-pyridone rings and 2-azetidinones. It is used as a formylating agent and used in the preparation of anti-poxvirus agents. It is used in Staudinger reaction and Hundsdiecker-barton iododecarboxylation reaction. It is widely used for studying organic photosensitizers, which finds application in dye-sensitized solar cells. | | Uses | Reagent or Reactant for the synthesis of: - β-Lactams vis the Staudinger reaction
- N-vinyl substituted indoles via cross coupling of NH-indoles with vinyl bromides
- Multi ring-fused 2-pyridone-based fluorescent scaffold
- ester prodrugs as anti-poxvirus agents
- Trimethine cyanine dyes for sensing G-quadruplex formation
- Phospha-isosteres via Hundsdiecker-Barton iododecacarboxylation
- 2-Azetidinones via [2+2]-cycloaddition
Used for studying organic photosensitizers for application in dye-sensitized solar cells |
| (Chloromethylene)dimethyliminium chloride Preparation Products And Raw materials |
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