N-Methoxy-N-methyl-1H-imidazole-1-carboxamide

Base Information

• Chemical Name: N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
• CAS No.: 862873-06-1
• Molecular Formula: C6H9N3O2
• Molecular Weight: 155.15
• European Community (EC) Number: 695-597-3
• Nikkaji Number: J2.888.202E

Synonyms:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide;862873-06-1;N-METHOXY-N-METHYLIMIDAZOLE-1-CARBOXAMIDE;SCHEMBL17154289;MFCD21608484;AKOS019064135;BS-51453;M2558;A914838;N-Methoxy-N-methyl-1H-imidazole-1-carboxamide, 95%

Chemical Property of N-Methoxy-N-methyl-1H-imidazole-1-carboxamide

Chemical Property:

• XLogP3: 0
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 155.069476538
• Heavy Atom Count: 11
• Complexity: 151

Purity/Quality:

97% ^*data from raw suppliers

N-Methoxy-N-methyl-1H-imidazole-1-carboxamide 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

• Canonical SMILES: CN(C(=O)N1C=CN=C1)OC
• Uses: N-Methoxy-N-methyl-1H-imidazole-1-carboxamide (or N-methoxy-N-methylcarbamoylimidazole) can be used as a reagent to prepare: N-methoxy-N-methylcyanoformamide by reacting with trimethylsilyl cyanide. Esters and amides via chemoselective esterification and amidation of carboxylic acids. Carbamoylimidazolium iodides and their derivatives such as ureas, thioureas, carbamates, and amides upon reacting with amines, alcohols, thiols, and carboxylic acids.

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