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Thermo Scientific Chemicals
Methyl carbazate, 98%
CAS: 6294-89-9 | C2H6N2O2 | 90.08 g/mol
化学物質識別子
CAS6294-89-9
IUPAC Namemethoxycarbohydrazide
Molecular FormulaC2H6N2O2
InChI KeyWFJRIDQGVSJLLH-UHFFFAOYSA-N
SMILESCOC(=O)NN
さらに表示
仕様
スペックシート
スペックシートFormCrystals or platelets or powder or crystalline powder
Melting Point (clear melt)68-73°
Appearance (Color)White to pale cream to pink
Assay (GC)≥97.5%
Methyl carbazate was used in the preparation of methyl 3-(4-methyl-benzyl-idene)carbazate. It was also used in the synthesis of imidazo[1,5-d][1,2,4]triazines. It is used as pharmaceutical intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Methyl carbazate was used in the preparation of methyl 3-(4-methyl-benzyl-idene)carbazate. It was also used in the synthesis of imidazo[1,5-d][1,2,4]triazines. It is used as pharmaceutical intermediate.
Solubility
Soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
Methyl carbazate was used in the preparation of methyl 3-(4-methyl-benzyl-idene)carbazate. It was also used in the synthesis of imidazo[1,5-d][1,2,4]triazines. It is used as pharmaceutical intermediate.
Solubility
Soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Matsuo Nonoyama. Pyrrole ring cyclopalladation of hydrazones derived from N-(p-toluenesulfonyl)-3-acetylpyrrole with acetylhydrazine, methyl carbazate and semicarbazide. Inorganica Chimica Acta. 1988, 145, (1),53-56
- R.Truhaut; R.Ferrando; J.M.Faccini; A.M.Monro. Negative results of carcinogenicity bioassay of methyl carbazate in rats: significance for the toxicological evaluation of carbadox. Toxicology. 1981, 22, (3),219-221
- Can be used in a sequence for converting ketones to homologated nitriles: Org. Synth. Coll:, 6, 334 (1988):
- Alternatively, reaction of the diazene intermediate with MeI and LiOMe yields the ɑ-methylnitrile: J. Org. Chem., 42, 2001 (1977).