34028-17-6

Basic information

• Product Name: N-methylbenzamidine
• Synonyms: N-methylbenzamidine;N1-Methylbenzamidine
• CAS NO: 34028-17-6
• Molecular Formula: C₈H₁₀N₂
• Molecular Weight: 134.18
• Mol File: 34028-17-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 242.7°Cat760mmHg
• Flash Point: 100.6°C
• Appearance: /
• Density: 1g/cm³
• CAS DataBase Reference: N-methylbenzamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-methylbenzamidine(34028-17-6)
• EPA Substance Registry System: N-methylbenzamidine(34028-17-6)

Safety Data

• Hazardous Substances Data: 34028-17-6(Hazardous Substances Data)

Upstream product

• 3409-96-9 benzenesulfonyl-benzoyl-methyl-amine 
• 19402-64-3 ammonium benzenesulfonate 
• 2397-29-7 N-methyl-N′-phenylbenzimidamide 
• 88070-48-8 N-methylbenzamide 
• 100-47-0 benzonitrile 
• 74-89-5 methylamine 
• 5333-86-8 ethyl benzimidate hydrochloride 

Downstream Products

• 25092-88-0 N¹,N²,N³-trimethylbenzamidine 
• 860684-83-9 N-bromo-N'-methyl-benzamidine 
• 67565-28-0 3-methyl-4-phenyl-2,2,6,6-tetrakis-trifluoromethyl-3,6-dihydro-2H-[1,3,5]oxadiazine 
• 78817-43-3 1-methyl-2-(4-methylphenyl)-4,6-diphenyl-1,2-dihydro-s-triazine 
• 78817-42-2 1-methyl-2,4,6-triphenyl-1,2-dihydro-1,3,5-triazine 
• 124911-04-2 N-Methyl-N'-(2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-1-imino-heptyl)-benzamidine 
• 74058-00-7 2-Phenyl-4,6-diperfluorohexyl-1,3,5-triazine 
• 97938-64-2 (4R,5R)-3-Methyl-2,5-diphenyl-4,5-dihydro-3H-imidazole-4-carboxylic acid ethyl ester 
• 97938-64-2 (4R,5S)-3-Methyl-2,5-diphenyl-4,5-dihydro-3H-imidazole-4-carboxylic acid ethyl ester 
• 20548-18-9 N,N-Dimethyl-benzamidine 
• 29019-38-3 N,N'-dimethylbenzoamidine 
• 857676-10-9 3-methyl-2-phenyl-3H-indeno[2,1-d]imidazol-8-one 

Relevant articles and documents

Copper-Catalyzed Intramolecular C-H Amination: A New Entry to Substituted Xanthine Derivatives

Catalytic synthesis of xanthines was achieved in the presence of a copper catalyst. The process involves copper-catalyzed intramolecular C-H amination of benzamidines that possess a uracil moiety and produces variously substituted xanthines generally in good to high yields. This work introduces a new, facile approach to polysubstituted xanthine compounds..

Research on 1,2,4-oxadiazol-5-ones. II. 4-Alkyl- and 4-acyl-1,2,4-oxadiazol-5-ones

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