340816-70-8

Basic information

• Product Name: 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid
• Synonyms: 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid
• CAS NO: 340816-70-8
• Molecular Weight: 270.312
• Mol File: 340816-70-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid(340816-70-8)
• EPA Substance Registry System: 3-amino-6-phenylthieno[2,3-b]pyridine-2-carboxylic acid(340816-70-8)

Safety Data

• Hazardous Substances Data: 340816-70-8(Hazardous Substances Data)

Upstream product

• 40381-90-6 2,6-dichloro-3-pyridinecarbonitrile 
• 1201-93-0 1-phenyl-3-dimethylaminoprop-2-enone 
• 98-86-2 acetophenone 
• 115919-87-4 3-Amino-6-phenyl-thieno<2,3-b>pyridin-2-carbonsaeureethylester 
• 92126-72-2 6-phenyl-2-thioxo-1,2-dihydropyridine-3-carbonitrile 
• 310456-47-4 [(3-cyano-6-phenylpyridin-2-yl)sulfanyl]acetic acid 

Downstream Products

• 1374993-92-6 2-methyl-3,7-diphenylpyrido[3',2':4,5]thieno[3,2-d]pyrimidin-4(3H)-one 
• 1374993-93-7 2-methyl-3-(4-methylphenyl)-7-phenylpyrido[3',2':4,5]thieno[3,2-d]pyrimidin-4-(3H)-one 
• 1374993-98-2 3-amino-2-methyl-7-phenylpyrido[3',2':4,5]thieno[3,2-d]pyrimidin-4(3H)-one 
• 132360-10-2 2-methyl-7-phenyl-4H-pyrido[3',2':4,5]thieno[3,2-d][1,3]oxazin-4-one 
• 1136717-48-0 C₁₈H₁₇N₃O₂S 

Relevant articles and documents

Identification of thienopyridine carboxamides as selective binders of HIV-1: Trans Activation Response (TAR) and Rev Response Element (RRE) RNAs

Small organic molecules that can selectively bind to RNA with specificity are relatively rare. Here we report the synthesis, biochemical and structural studies of thienopyridine carboxamide derivatives with the capacity of selectively recognizing and binding with HIV-1 TAR and RRE RNAs that are essential elements for viral replication.

Synthesis and characterization of 6-(aryl)-2-thioxo-1,2-dihydropyridine-3- carbonitriles

In the present study, 3-aminothieno[2,3-b]pyridines, pyrido[3′, 2′:4,5]thieno[3,2-d]pyrimidinones, and pyrido[3′,2′:4,5] thieno[3,2-d][1,3]oxazinones were prepared via the reaction of 6-(aryl)-2-thioxo-1,2-dihydropyridine-3-carbonitriles with active-halog