102423-20-1

Basic information

• Product Name: Benzenecarboximidic acid, 4-chloro-N-cyano-, methyl ester
• CAS NO: 102423-20-1
• Molecular Formula: C9H7ClN2O
• Molecular Weight: 194.62
• Mol File: 102423-20-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidic acid, 4-chloro-N-cyano-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidic acid, 4-chloro-N-cyano-, methyl ester(102423-20-1)
• EPA Substance Registry System: Benzenecarboximidic acid, 4-chloro-N-cyano-, methyl ester(102423-20-1)

Safety Data

• Hazardous Substances Data: 102423-20-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 420-04-2 CYANAMID 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 114113-41-6 C₁₂H₁₂ClN₃OS 
• 114113-49-4 C₁₀H₁₀ClN₃OS 
• 111268-25-8 N¹-(Benzylethylimino-λ⁶-sulfanyliden)-4-chlor-N²-cyanbenzamidin 
• 114565-04-7 4-Chlor-N²-cyan-N¹-(tetrahydro-1-imino-λ⁶-thiophen-1-yliden)benzamidin 
• 1196908-62-9 C₁₄H₁₁ClN₄ 
• 1478440-55-9 4-chloro-N-[(diphenylamino)(imino)methyl]benzamide 
• 223685-95-8 4-chloro-N-[2,3-dihydro-1H-indol-1-yl(imino)methyl]benzamide 
• 54434-01-4 N-[anilino(imino)methyl]-4-chlorobenzamide 
• 1478440-33-3 C₁₄H₁₀ClN₃ 
• 114113-62-1 3,6-Bis-(4-chloro-phenyl)-1-methyl-1-oxo-1λ⁶-pyrimido[4,5-e][1,2,4]thiadiazin-8-ylamine 
• 114113-57-4 5-(4-Chloro-phenyl)-3a-oxo-3aλ⁶-thia-4,6-diaza-indan-7-ylamine 
• 111268-48-5 1-<5-(4-Chlorphenyl)-1-ethyl-1λ⁴,2,4,6-thiatriazin-3-yl>-3-phenylharnstoff 
• 111268-40-7 5-(4-Chlorphenyl)-1-ethyl-1λ⁴,2,4,6-thiatriazin-3-amin 
• 114565-27-4 2-(4-Chlorphenyl)-6,7-dihydro-8-(methylsulfonylimino)-5H-thieno<2,1-f><1λ⁶,2,4>thiadiazin-4-amin 

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.