86700-29-0

Basic information

• Product Name: Benzenecarboximidic acid, N-cyano-4-methyl-, methyl ester
• CAS NO: 86700-29-0
• Molecular Formula: C10H10N2O
• Molecular Weight: 174.202
• Mol File: 86700-29-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidic acid, N-cyano-4-methyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidic acid, N-cyano-4-methyl-, methyl ester(86700-29-0)
• EPA Substance Registry System: Benzenecarboximidic acid, N-cyano-4-methyl-, methyl ester(86700-29-0)

Safety Data

• Hazardous Substances Data: 86700-29-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 420-04-2 CYANAMID 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 102423-24-5 <2-(Dimethyloxo-λ⁶-sulfanyliden)-1-(4-methylphenyl)ethyliden>cyanamid 
• 102423-38-1 1-<1-Methyl-5-(4-methylphenyl)-1λ⁴,4-thiazin-3-yl>-3-phenylharnstoff-S-oxid 
• 102423-32-5 1-Methyl-5-(4-methylphenyl)-1λ⁴,4-thiazin-3-amin-1-oxid 
• 1196908-58-3 C₁₅H₁₄N₄ 
• 96237-41-1 4-methoxy-5-phenylsulphonyl-6-(p-tolyl)pyrimidin-2-amine 
• 96237-37-5 2-methoxy-5-phenylsulphonyl-6-(p-tolyl)pyrimidin-4-amine 
• 96237-25-1 3-<(aminocarbonyl)amino>-2-(phenylsulphonyl)-3-(p-tolyl)propenenitrile 
• 96237-29-5 4-amino-5-phenylsulphonyl-6-(p-tolyl)pyrimidin-2(1H)-one 
• 114113-61-0 1-Methyl-1-oxo-3,6-di-p-tolyl-1λ⁶-pyrimido[4,5-e][1,2,4]thiadiazin-8-ylamine 
• 114113-56-3 3a-Oxo-5-p-tolyl-3aλ⁶-thia-4,6-diaza-indan-7-ylamine 
• 111268-47-4 1-<1-Ethyl-5-(4-methylphenyl)-1λ⁴,2,4,6-thiatriazin-3-yl>-3-phenylharnstoff 
• 111268-39-4 1-Ethyl-5-(4-methylphenyl)-1λ⁴,2,4,6-thiatriazin-3-amin 
• 107326-02-3 7-(4-Chlorphenyl)-5-methyl-2-p-tolylpyrimido<5,4-b><1λ⁴,4>thiazin-4-amin-5-oxid 
• 111268-21-4 N²-Cyan-4-methyl-N¹-(tetrahydro-1-imino-λ⁶-thiophen-1-yliden)benzamidin 

Relevant articles and documents

Highly efficient cyanoimidation of aldehydes

"Chemical Equation Presented" Cyanoimidation of aldehydes using cyanamide as a nitrogen source and using NBS as an oxidant was achieved in high yields without the addition of a catalyst. The method has several advantages, Including mild conditions, simple workflow, and inexpensive reagents. The reaction proceeds in a one-pot manner, giving rise to the formation of intermolecular C-N and C-O bonds. Subsequently, the substituted W-cyanobenimidate products may also undergo a cyclization reaction to give 1,2,4-triazole derivatives in high yields.