1452517-10-0

Basic information

• Product Name: ethanimidamide, N,N'-diphenyl-, (1E)-
• Synonyms: (1E)-N,N'-diphenylethanimidamide;ethanimidamide, N,N'-diphenyl-, (1E)-;4-12-00-00384 (Beilstein Handbook Reference);Acetamidine, N,N'-diphenyl-;BRN 2804188;EINECS 210-669-2;Ethanimidamide, N,N'-diphenyl-;MLS000105031
• CAS NO: 1452517-10-0
• Molecular Formula: C14H14N2
• Molecular Weight: 210.27436
• Mol File: 1452517-10-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ethanimidamide, N,N'-diphenyl-, (1E)-(CAS DataBase Reference)
• NIST Chemistry Reference: ethanimidamide, N,N'-diphenyl-, (1E)-(1452517-10-0)
• EPA Substance Registry System: ethanimidamide, N,N'-diphenyl-, (1E)-(1452517-10-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1452517-10-0(Hazardous Substances Data)

Upstream product

• 98-07-7 Benzotrichlorid 
• 103-84-4 Acetanilid 
• 16900-53-1 3-bromopropiolic acid 
• 62-53-3 aniline 
• 56-23-5 tetrachloromethane 
• 3460-08-0 N¹-benzoyl-N¹,N²-diphenylacetamidine 
• 100-09-4 4-methoxybenzoic acid 
• 108-42-9 3-chloro-aniline 
• 5504-03-0 N¹-tosyl-N¹,N²-diphenylacetamidine 
• 74-86-2 acetylene 

Downstream Products

• 130685-40-4 2,3-Dihydro-2-(methyl-phenylamin-methylen)-3-oxo-benzothiophen-1,1-dioxid 
• 64-19-7 acetic acid 
• 62-53-3 aniline 
• 51452-80-3 (n-C₃H₇)2BNC₆H₅C(=NC₆H₅)(CH₃) 
• 71395-48-7 Rh(η5-pentamethylcyclopentadienyl)Cl(N,N'-diphenylacetamidinato) 
• 89516-75-6 C₁₅H₁₃N₃O₃S 
• 99806-16-3 4-ethyl-1-phenyl-2-phenylimino-cis-3a,4,9,9a-tetrahydro-3H-pyrrole<2,3-b>quinoxaline 
• 61201-42-1 3,6-Dihydro-2,5-dimethyl-6-oxo-1,3-diphenyl-1-pyrimidinium-4-olat 
• 71382-70-2 3-methylene-2,4-diphenyl-3,4-dihydro-2H-furo[3,4-e][1,3]diazepine-1,5-dione 
• 2385-23-1 2-Methyl-3-phenyl-4(3H)-quinazolinone 
• 186193-55-5 PdCl₂(P((CH₂)3CH₃)3)(C₆H₅NC(CH₃)NHC₆H₅) 
• 186193-60-2 PdCl₂(P(C₆H₅)2CH₃)(C₆H₅NC(CH₃)NHC₆H₅) 
• 186193-59-9 PdCl₂(P(C₆H₅)2CH₃)(C₆H₅NC(CH₃)NHC₆H₅) 
• 186193-67-9 PtCl₂(P(CH₃)2C₆H₅)(C₆H₅NC(CH₃)NHC₆H₅) 

Relevant articles and documents

Hydrolysis of Acyl Derivatives of N1,N2-Diarylamidine. I

The alkaline hydrolyses of N1-benzoyl-N1,N2-diarylacetamidine (V) and N1-tosyl-N1,N2-diarylacetamidine (IX) were examined.In the hydrolysis of V, hydroxide ion attacked the amide carbonyl carbon to form N1,N2-diarylacetamidine and benzoic acid.In the hydrolysis of IX, hydroxide ion attacked the amidine carbon, and elimination of the N-tosylarylamino group and arylimino group proceeded in parallel, with that of the latter predominating.The alcoholysis reaction of V proceeded without any added catalyst, in contrast to the case of 1-(N-benzoylarylamino)-3-arylimino-1-propene.A unique peak corresponding to the loss of 64 mass units (sulfur dioxide) was observed in the mass spectrum of IX.Keywords - alkaline hydrolysis; alcoholysis; N1-benzoyl-N1,N2-diarylacetamidine; N1-tosyl-N1,N2-diarylacetamidine; 1,1-bis(N-benzoylarylamino)ethene; MS

Catalytic and Non-catalytic Addition of Aromatic Amines to Terminal Acetylenes in the Presence of Mercury(II) Chloride and Acetate

The addition of aromatic amines to terminal acetylenes in the presence of catalytic amounts of mercury(II) chloride gives imines, enamines, and 1,2,3,4-tetrahydroquinoline derivatives; mercury(II) acetate shows considerably less catalytic activity and may be used for the non-catalytic preparation of imines, enamines, N,N'-disubstituted acetamidines, and N,N-disubstituted acetamides.