58327-71-2

Basic information

• Product Name: Thieno[2,3-b]pyridine-2-carbonitrile, 3-amino-4,6-diphenyl-
• CAS NO: 58327-71-2
• Molecular Formula: C20H13N3S
• Molecular Weight: 327.409
• Mol File: 58327-71-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Thieno[2,3-b]pyridine-2-carbonitrile, 3-amino-4,6-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Thieno[2,3-b]pyridine-2-carbonitrile, 3-amino-4,6-diphenyl-(58327-71-2)
• EPA Substance Registry System: Thieno[2,3-b]pyridine-2-carbonitrile, 3-amino-4,6-diphenyl-(58327-71-2)

Safety Data

• Hazardous Substances Data: 58327-71-2(Hazardous Substances Data)

Upstream product

• 78564-27-9 2-Cyanomethylsulfanyl-4,6-diphenyl-nicotinonitrile 
• 120-46-7 1,3-diphenylpropanedione 
• 94-41-7 benzalacetophenone 
• 62940-90-3 2-(3-oxo-1,3-diphenylpropyl)malononitrile 
• 82127-26-2 2-bromo-4,6-diphenylpyridine-3-carbonitrile 
• 58327-74-5 4,6-diphenyl-2-thioxo-1,2-dihydropyridine-3-carbonitrile 
• 107-14-2 chloroacetonitrile 
• 58327-74-5 4,6-diphenyl-2-mercaptonicotinonitrile 

Downstream Products

• 217954-57-9 (4-Chloro-7,9-diphenyl-pyrido[3',2':4,5]thieno[3,2-d]pyrimidin-2-yl)-dimethyl-amine 
• 217954-49-9 3-chlorodimethylaminomethylenamino-2-cyano-4,6-diphenylthieno[2,3-b]pyridine 
• 151058-81-0 4-Chloro-7,9-diphenyl-pyrido[3',2':4,5]thieno[3,2-d][1,2,3]triazine 

Relevant articles and documents

Synthesis of some new pyrido[3',2':4,5]thieno[3,2-d[1,2,3-triazines with antianaphylactic activity

Some new pyrido[3',2':4,5]thieno[3,2-d]1,2,3-triazine-4(3H)-ones (C) were synthesized from 2-thioxo-1,2-dihydro-3-carbonitriles (A) via the 3-amino-thieno[2,3-b]pyridine-2-carboxamides (B). Substances of structure A were converted to 3-amino-thieno[2,3-b]

SYNTHESIS AND SOME REACTIONS OF 3-CYANOPYRIDINE-2-THIONES

New method for the synthesis of 3-cyanopyridine-2-thiones by the reaction of δ-keto nitroles with sulfur and by condensation of chalcones or benzylideneacetone with cyanothioacetamide are given.The compounds obtained were used in various reactions for the preparation of alkylated products, disulfides, and condensed heterocycles, viz., thienopyridines and pyridothienopyrimidines.