4847-47-6

Basic information

• Product Name: 2-Propenenitrile, 3-phenyl-3-(phenylamino)-
• CAS NO: 4847-47-6
• Molecular Formula: C15H12N2
• Molecular Weight: 220.274
• Mol File: 4847-47-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propenenitrile, 3-phenyl-3-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenenitrile, 3-phenyl-3-(phenylamino)-(4847-47-6)
• EPA Substance Registry System: 2-Propenenitrile, 3-phenyl-3-(phenylamino)-(4847-47-6)

Safety Data

• Hazardous Substances Data: 4847-47-6(Hazardous Substances Data)

Upstream product

• 70801-58-0 2-Cyano-3-phenyl-4H-benzo<1,4>thiazine 
• 614-16-4 Benzoylacetonitrile 
• 62-53-3 aniline 
• 4492-01-7 1,3-diphenyl-1H-pyrazole 
• 64-17-5 ethanol 
• 935-02-4 3-Phenyl-2-propynonitrile 
• 1823-99-0 3-amino-3-phenylacrylonitrile 
• 542-14-3 aniline acetate 
• 1270-67-3 4-amino-2,3-diphenylthiazolium chloride 

Downstream Products

• 614-16-4 Benzoylacetonitrile 
• 62-53-3 aniline 
• 51072-85-6 2-phenyl-1H-indole-3-carbonitrile 
• 59393-45-2 3-phenyl-2-quinoxalinecarbonitrile 
• 93-98-1 N-phenyl benzoyl amide 
• 117266-86-1 4-cyano-1,5-diphenyl-3-ethoxy-3-hydroxy-pyrrole-2-one 
• 72694-08-7 (Z)-2-Cyano-3-phenyl-3-phenylamino-dithioacrylic acid ethyl ester 
• 117266-85-0 4-cyano-1,5-diphenyl-pyrrole-2,3-dione 

Relevant articles and documents

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PIDA-mediated oxidative C-C bond formation: Novel synthesis of indoles from n-aryl enamines

A variety of functionalized indoles were synthesized from N-aryl enamines via PIDA-mediated oxidative carbon-carbon bond formation. The features of the present reaction include facilitative preparation of substrates 2, good functional group tolerance, and mild reaction conditions without transition metals.

Adducts of 2-aminothiophenol with acetylenic nitriles or esters and their conversion into benzothiazoles and/or 1,4-benzothiazines

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