6041-23-2

Basic information

• Product Name: N-CYANOBENZIMIDIC METHYL ESTER
• Synonyms: N-CYANOBENZIMIDIC METHYL ESTER;methyl N-cyanobenzimidate;N-Cyanobenzenecarbimidic acid methyl ester;1g 5g 10g;BenzenecarboxiMidic acid;HUJTXVINLQYRNH-PKNBQFBNSA-N
• CAS NO: 6041-23-2
• Molecular Formula: C₉H₈N₂O
• Molecular Weight: 160.17
• EINECS: 227-927-5
• Mol File: 6041-23-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 237°C at 760 mmHg
• Flash Point: 97.1°C
• Appearance: /
• Density: 1.02g/cm³
• Vapor Pressure: 0.0459mmHg at 25°C
• Refractive Index: 1.522
• PKA: -4.14±0.50(Predicted)
• CAS DataBase Reference: N-CYANOBENZIMIDIC METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: N-CYANOBENZIMIDIC METHYL ESTER(6041-23-2)
• EPA Substance Registry System: N-CYANOBENZIMIDIC METHYL ESTER(6041-23-2)

Safety Data

• Hazardous Substances Data: 6041-23-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H8N2O/c1-12-9(11-7-10)8-5-3-2-4-6-8/h2-6H,1H3/b11-9-

Upstream product

• 420-04-2 CYANAMID 
• 707-07-3 orthobenzoic acid trimethyl ester 
• 67-56-1 methanol 
• 100-52-7 benzaldehyde 
• 5873-90-5 methyl benzimidate hydrochloride 

Downstream Products

• 51742-77-9 6β-[(N-cyano-benzimidoyl)-amino]-penicillanic acid 2,2-dimethyl-propionyloxymethyl ester 
• 96280-50-1 4-Chloro-6-phenyl-5-phenylsulphonylpyrimidin-2-amine 
• 96237-28-4 4-amino-6-phenyl-5-phenylsulphonylpyrimidin-2(1H)-one 
• 96237-23-9 3-<(aminocarbonyl)amino>-3-phenyl-2-(phenylsulphonyl)propenenitrile 
• 96237-36-4 2-methoxy-6-phenyl-5-phenylsulphonylpyrimidin-4-amine 
• 96237-40-0 4-methoxy-6-phenyl-5-phenylsulphonylpyrimidin-2-amine 
• 7788-14-9 5-phenyl-1,2,4-oxadiazol-3-amine 
• 3663-37-4 3-phenyl-1,2,4-oxadiazol-5-amine 
• 41813-97-2 1,3-diphenyl-1,2,4-triazol-5-amine 
• 86700-28-9 2-Amino-4-phenyl-6-thioxo-1,6-dihydro-pyrimidine-5-carbonitrile 
• 31709-26-9 ethyl [5-phenyl-1,2,4-oxadiazol-3-yl]imidoformate 
• 81066-94-6 2-amino-1,6-dihydro-6-oxo-4-phenylpyrimidine-5-carbonitrile 
• 86700-23-4 Bis<2-amino-6-phenyl-5-cyanopyrimidin-4-yl> disulfide 
• 30369-38-1 2-amino-4-methoxy-6-phenyl-1,3,5-triazine 

Relevant articles and documents

HETEROCYCLIC COMPOUNDS AS PESTICIDES

The present application relates to novel heterocyclic compounds, to the use thereof for controlling animal pests including arthropods, insects and nematodes, and to processes and intermediates for preparation of the novel compounds.

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.