4636-51-5

Basic information

• Product Name: N,N-dibenzylmethanimidamide
• CAS NO: 4636-51-5
• Molecular Formula: C₁₅H₁₆N₂
• Molecular Weight: 224.305
• Mol File: 4636-51-5.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 363.9°Cat760mmHg
• Flash Point: 173.9°C
• Density: 0.99g/cm³
• CAS DataBase Reference: N,N-dibenzylmethanimidamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dibenzylmethanimidamide(4636-51-5)
• EPA Substance Registry System: N,N-dibenzylmethanimidamide(4636-51-5)

Safety Data

• Hazardous Substances Data: 4636-51-5(Hazardous Substances Data)

Upstream product

• 290-87-9 1,3,5-Triazine 
• 100-46-9 benzylamine 
• 16694-46-5 ethyl formimidate hydrochloride 
• 97769-04-5 N,N'-Dibenzyl-N-dichlormethyl-formamidiniumchlorid 
• 122-51-0 orthoformic acid triethyl ester 
• 124-38-9 carbon dioxide 
• 1466-67-7 1,3-dibenzylurea 
• 1424-14-2 dibenzyl thiourea 
• 34669-83-5 N-(n-Butyl)-carbamimidoylameisensaeure 
• 55152-76-6 N,N'-Dibenzyl-formamidin-sulfinsaeure 

Downstream Products

• 84206-39-3 [Os₃H₂(CO)9(C₆H₄CH₂NCHNCH₂C₆H₅)] 
• 84206-38-2 [Os₂(CO)6(C₆H₅CH₂NCHNCH₂C₆H₅)2] 

Relevant articles and documents

Hree-component reaction of benzylamines, diethyl phosphite and triethyl orthoformate: Dependence of the reaction course on the structural features of the substrates and reaction conditions

The reaction between benzyl amines, triethyl orthoformate, and diethyl phosphite affords either bisphosphonic (compound 1) or N-benzylaminobenzylphosphonic (compound 2) acid depending on the reaction conditions. The final output of the reaction can be manipulated by the choice of reaction conditions, particularly the molar ratio of substrates.

Method For Preparing Nitrogen Compounds

The present invention relates to a method for preparing nitrogen compounds using carbon dioxide, and to the use of the method in the production of vitamins, pharmaceutical products, adhesives, acrylic fibres, synthetic leathers, pesticides, herbicides, antifungal agents and fertilisers. The invention also relates to a method for producing vitamins, pharmaceutical products, adhesives, acrylic fibres, synthetic leathers, pesticides, herbicides, antifungal agents and fertilisers, which includes a step of preparing nitrogen compounds using the method of the invention. The invention further relates to a method for preparing labelled nitrogen compounds using carbon dioxide and to the uses thereof.

Pushing back the limits of hydrosilylation: Unprecedented catalytic reduction of organic ureas to formamidines

Pushing back the limits: A novel catalytic transformation has been designed to prepare formamidine derivatives by reduction of substituted ureas with hydrosilanes. Simple iron catalysts based on commercially available iron salts and phosphine ligands prov