14277-00-0

Basic information

• Product Name: Ethanimidamide,N-phenyl-
• Synonyms: Acetamidine,N-phenyl- (6CI,8CI); N-Phenylacetamidine
• CAS NO: 14277-00-0
• Molecular Formula: C8H10 N2
• Molecular Weight: 134.181
• Mol File: 14277-00-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 242.7°Cat760mmHg
• Flash Point: 100.6°C
• Density: 1g/cm³
• CAS DataBase Reference: Ethanimidamide,N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanimidamide,N-phenyl-(14277-00-0)
• EPA Substance Registry System: Ethanimidamide,N-phenyl-(14277-00-0)

Safety Data

• Hazardous Substances Data: 14277-00-0(Hazardous Substances Data)

Upstream product

• 625-77-4 N-acetylacetamide 
• 142-04-1 aniline hydrochloride 
• 542-11-0 aniline hydrobromide 
• 75-05-8 acetonitrile 
• 62-53-3 aniline 
• 167780-26-9 {1-[(Z)-Benzyloxycarbonylimino]-ethyl}-carbamic acid benzyl ester 
• 7647-01-0 hydrogenchloride 
• 60-29-7 diethyl ether 
• 71-43-2 benzene 
• 4484-20-2 aniline benzenesulfonate 
• 105-56-6 ethyl 2-cyanoacetate 
• 591-50-4 iodobenzene 
• 124-42-5 acetamidine hydrochloride 
• 23228-59-3 2,2,2-trichloroethyl acetimidate 

Downstream Products

• 109510-70-5 N-phenyl-N'-(N-phenyl-acetimidoyl)-thiourea 
• 6899-38-3 3-methyl-1-(toluene-4-sulfonylamino)-1λ⁴-benzo[1,2,4]thiadiazine 
• 89646-90-2 4-(2-Methyl-1,5-diphenyl-4,5-dihydro-1H-imidazol-4-yl)-morpholine 
• 32363-53-4 2,6-dimethyl-3-phenyl-4(3H)-pyrimidinone 
• 87356-66-9 2-methyl-3,6-diphenylpyrimidin-4(3H)-one 
• 1002107-31-4 2-methyl-1-phenyl-1H-imidazole-5-carbaldehyde 
• 1352641-86-1 [(CH₃)5Al₄(N(C₆H₅)C(CH₃)N)4H] 
• 1352641-86-1 [(CH₃)5Al₄(N(C₆H₅)C(CH₃)N)4H] 
• 1207066-26-9 N¹-phenylacetamidine 4-bromobenzoate 
• 1484-39-5 2-methyl-1-phenyl-1H-benzimidazole 
• 23974-78-9 2-benzylquinoline 1-oxide 
• 1745-77-3 2-benzylquinoline 
• 1379771-31-9 2-(4-bromobenzyl)quinoline 
• 1613-41-8 2-phenethyl-quinoline 

Relevant articles and documents

N,N'-bis(benzyloxycarbonyl)acetamidine, a versatile reagent for the conversion of amines and alcohols to acetamidines

N,N'-bis(benzyloxycarbonyl)acetamidine is the prototype of a new class of versatile reagents for the conversion of amines and alcohols to substituted amidines. The preparation of 1 and its potential uses are described.

Ligand-free copper-catalyzed arylation of amidines

Copper-catalyzed cross-coupling reactions of amidine salts were utilized to synthesize monoarylated amidines in moderate to high yields with ligand-free conditions. DMF was the superior solvent for the N-arylation of benzamidines, while MeCN was used in the formation of N-aryl amidines in moderate to high yield.(Figure Presented)

Electrochemical behavior of amidine hydrochlorides and amidines

The electrochemical behavior of N,N-dimethyl-N'-phenylformamidine hydrochloride was studied on a platinum electrode.The oxidation peak at +0.90 V vs.Ag/Ag+ 0.01 M (in CH3CN - 0.1 M LiClO4) was assigned to the oxidation of the chloride anion.N,N