4450-64-0

Basic information

• Product Name: Benzenecarboximidamide, 4-methoxy-N-phenyl-
• CAS NO: 4450-64-0
• Molecular Formula: C14H14N2O
• Molecular Weight: 226.278
• Mol File: 4450-64-0.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidamide, 4-methoxy-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidamide, 4-methoxy-N-phenyl-(4450-64-0)
• EPA Substance Registry System: Benzenecarboximidamide, 4-methoxy-N-phenyl-(4450-64-0)

Safety Data

• Hazardous Substances Data: 4450-64-0(Hazardous Substances Data)

Upstream product

• 874-90-8 4-methoxybenzonitrile 
• 62-53-3 aniline 
• 622-73-1 4-methoxybenzaldehydephenylhydrazone 
• 51721-68-7 4-methoxybenzamidine hydrochloride 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 45821-44-1 4-methoxy-benzylideneamine 
• 622-37-7 Phenyl azide 
• 3424-93-9 4-methoxyphenylacetamide 

Downstream Products

• 51-66-1 4-methoxyacetanilide 
• 935750-33-7 5-ethyl-2,4-bis(4-methoxyphenyl)-1-phenyl-1H-imidazole 
• 2620-81-7 2-(4-methoxyphenyl)-1H-benzimidazole 
• 1242182-96-2 2-(4-methoxyphenyl)-4-[(triisopropylsilyl)methyl]quinazoline 
• 1177129-70-2 N-tert-butyl-4-amino-2-(4-methoxyphenyl)quinazoline 
• 1152-07-4 2-(4-methoxyphenyl)-3H-quinazolin-4-one 
• 1602636-82-7 C₂₃H₂₀N₂O 
• 1602636-73-6 2-(4-methoxyphenyl)-1,4-diphenyl-1H-imidazole 
• 67205-04-3 2-(4-methoxyphenyl)quinazoline 
• 93-98-1 N-phenyl benzoyl amide 
• 77290-63-2 N-benzoyl-4-methoxy-o-anisamide 

Relevant articles and documents

Combination of air/moisture/ambient temperature compatible organolithium chemistry with sustainable solvents: Selective and efficient synthesis of guanidines and amidines

Highly-efficient and selective fast addition of in situ generated lithium amides [LiN(H)R] (obtained via an acid-base reaction between n-BuLi and the desired primary amine) into carbodiimides (R-NCN-R) or nitriles (R-CN) has been studied, for the first ti

Intramolecular hydrogen bonding stabilizes trans-configuration in a mixed carbene/isocyanide PdII complexes

Aromatic amidines 1a-e undergo facile reaction with one isocyanide in PdCl2(CNBut)2 giving carbene complexes 2b-d (Scheme 2) in high isolated yields (79–95%). The structures of 2b–d were confirmed by the 1H and

Metal-Free Synthesis of Polysubstituted Imidazolinone Through Cyclization of Amidines with 2-Substituted Acrylates

Polysubstituted imidazolinones were synthesized in a facile metal-free cascade nucleophilic cyclization of easily available amidines and 2-substituted acrylates. This protocol is distinguished by simple, mild, and catalyst-free reaction conditions with a broad substrate scope, affording the desired products in moderate to good yields and providing an efficient strategy for synthesis of polysubstituted imidazolinone.