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

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Company Name: Aladdin Scientific
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Products Intro: Product Name:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
CAS:862873-06-1
Purity:95.0%(GC) Package:$9.9/200mg;$32.9/1g;$110.9/5g;$375.9/25g;Bulk package Remarks:95.0%(GC)
Company Name: Amadis Chemical Company Limited
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Products Intro: Product Name:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
CAS:862873-06-1
Purity:0.97 Package:mgs,gs,kgs Remarks:A914838
Company Name: TOKYO CHEMICAL INDUSTRY CO., LTD.  
Tel: 03-36680489
Email: Sales-JP@TCIchemicals.com
Products Intro: Product Name:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
CAS:862873-06-1
Purity:95-98% Package:200 mg
Company Name: TCI Europe  
Tel: 320-37350700
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Products Intro: Product Name:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
CAS:862873-06-1
Purity:95-98% Package:200 mg
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 13681763483
Email: product02@bidepharm.com
Products Intro: Product Name:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
CAS:862873-06-1
Purity:97% Package:1g;5g;25g; Remarks:BD633529
N-Methoxy-N-methyl-1H-imidazole-1-carboxamide Basic information
Product Name:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide
Synonyms:N-Methoxy-N-methyl-1H-imidazole-1-carboxamide;WImC;1H-Imidazole-1-carboxamide, N-methoxy-N-methyl-;N-METHOXY-N-METHYL-1H-IMIDAZOLE-1-CARBO&
CAS:862873-06-1
MF:C6H9N3O2
MW:155.15
EINECS:
Product Categories:
Mol File:862873-06-1.mol
N-Methoxy-N-methyl-1H-imidazole-1-carboxamide Structure
N-Methoxy-N-methyl-1H-imidazole-1-carboxamide Chemical Properties
Boiling point 234.4±23.0 °C(Predicted)
density 1.204 g/mL at 25 °C
refractive index n20/D1.508
Fp >110℃
storage temp. 2-8°C
pka3.44±0.10(Predicted)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
MSDS Information
N-Methoxy-N-methyl-1H-imidazole-1-carboxamide Usage And Synthesis
UsesN-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.

N-Methoxy-N-methyl-1H-imidazole-1-carboxamide Preparation Products And Raw materials
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