CAS 1739-84-0
:1,2-Dimetilimidazol
- 1,2-dimethyl-1H-imidazole
- 1,2Dmz
- 1H-Imidazole, 1,2-dimethyl-
- Curezol 1,2DMZ
- Dabco 2039
- Dabco 2040
- Dabco 2041
- Imidazole, 1,2-dimethyl-
- Kaolizer 390
- Lupragen DMI
- N,2-Dimethylimidazole
- NSC 111174
- Nichigo Imidazole 1,2-DMI
- Pc Cat Dmi
- SN 25 (vulcanizing agent)
- Sn 25
- Toyocat DM 70
- Toyocat DMI
- Toyocat DP 70
- Ver más sinónimos
1,2-Dimethylimidazole
CAS:Fórmula:C5H8N2Pureza:>98.0%(GC)Forma y color:White or Colorless to Light yellow powder to lump to clear liquidPeso molecular:96.131,2-Dimethylimidazole, 98%
CAS:1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts. This Thermo Scientific Chemicals braFórmula:C5H8N2Pureza:98%Forma y color:Colorless to white to pale yellow, Crystals or powder or crystalline powder or fused solid or chunksPeso molecular:96.131,2-Dimethyl-1H-imidazole
CAS:1,2-Dimethyl-1H-imidazole is an imidazole derivative widely used in biochemical experiments and drug synthesis research.
Fórmula:C5H8N2Forma y color:SolidPeso molecular:96.131,2-Dimethyl-1H-imidazole 98%
CAS:1,2-Dimethyl-1H-imidazole 98%Pureza:≥95%Peso molecular:96.13042g/mol1,2-Dimethylimidazole
CAS:Fórmula:C5H8N2Pureza:99.00%Forma y color:Low Melting SolidPeso molecular:96.1331,2-Dimethylimidazole
CAS:Producto controladoApplications 1,2-DIMETHYLIMIDAZOLE (cas# 1739-84-0) is a useful research chemical.
Fórmula:C5H8N2Forma y color:Light Yellow To Light BeigePeso molecular:96.131,2-Dimethylimidazole
CAS:1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant.
Fórmula:C5H8N2Pureza:Min. 95%Forma y color:PowderPeso molecular:96.13 g/molRef: 3D-FD38774
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