6721-03-5

Basic information

• Product Name: N,N'-methanediylidenebis(1-phenylmethanamine)
• Synonyms: N,N'-methanediylidenebis(1-phenylmethanamine)
• CAS NO: 6721-03-5
• Molecular Weight: 222.29
• Mol File: 6721-03-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N,N'-methanediylidenebis(1-phenylmethanamine)(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-methanediylidenebis(1-phenylmethanamine)(6721-03-5)
• EPA Substance Registry System: N,N'-methanediylidenebis(1-phenylmethanamine)(6721-03-5)

Safety Data

• Hazardous Substances Data: 6721-03-5(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 1466-67-7 1,3-dibenzylurea 
• 88333-03-3 Benzyl isocyanide 
• 622-79-7 benzyl azide 
• 100-39-0 benzyl bromide 
• 3173-56-6 benzyl isothiocyanate 
• 71-43-2 benzene 
• 1424-14-2 dibenzyl thiourea 
• 622-78-6 Benzyl isothiocyanate 

Downstream Products

• 1466-67-7 1,3-dibenzylurea 
• 1415958-99-4 1,3-dibenzyl-5-ethylimidazolidine-2,4-dione 
• 92357-91-0 1,3-dibenzyl-1,3-diazaspiro[4.5]decane-2,4-dione 
• 1118749-90-8 1,3-dibenzyl-5-biphenyl-4-yl-imidazolidine-2,4-dione 
• 7461-34-9 N-benzyl-p-chlorobenzamide 
• 1485-70-7 N-benzylbenzamide 
• 2142-01-0 N-benzylphthalimide 
• 1428966-84-0 C₂₈H₃₁N₃O₄ 
• 1118749-84-0 1,3-dibenzyl-5-phenylimidazolidine-2,4-dione 
• 56383-54-1 3-benzyl-2-benzylimino-6-methylsulfanyl-2,3-dihydro-[1,3]thiazin-4-one 
• 78450-19-8 dibenzyl-1,3 thymine 
• 64643-56-7 C₁₉H₂₅N₂O₃PS 
• 81017-66-5 C₁₇H₂₁N₂O₂PS₂ 
• 76070-72-9 C₁₆H₁₈N₄S*2ClH 

Relevant articles and documents

Gram Scalable Method to Synthesize Biscarbodiimides and Asymmetric Monocarbodiimides: A Platform to Access an Array of Phosphaguanidines, Amidines, and Guanidines

A mild, broadly functional group tolerant methodology has been developed to access a variety of mono- and bis-carbodiimides in good yield and high purity on multigram scale. Direct addition into these versatile motifs facilitated the rapid synthesis of a library of novel amidinines, guanidines, and phosphaguandines.

Rhenium-Catalyzed Synthesis of 1,3-Diiminoisoindolines via Insertion of Carbodiimides into a C-H Bond of Aromatic and Heteroaromatic Imidates

The rhenium-catalyzed synthesis of 1,3-diiminoisoindolines and their related compounds from aromatic or heteroaromatic imidates and carbodiimides are reported via C-H bond activation. This reaction is the first example of a transition-metal-catalyzed inse

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