1261743-67-2

Basic information

• Product Name: 3-phenyl ethyl isonicotinate
• Synonyms: 3-phenyl ethyl isonicotinate
• CAS NO: 1261743-67-2
• Molecular Weight: 227.263
• Mol File: 1261743-67-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-phenyl ethyl isonicotinate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl ethyl isonicotinate(1261743-67-2)
• EPA Substance Registry System: 3-phenyl ethyl isonicotinate(1261743-67-2)

Safety Data

• Hazardous Substances Data: 1261743-67-2(Hazardous Substances Data)

Upstream product

• 1570-45-2 isonicotinic acid ethylester 
• 98-80-6 phenylboronic acid 
• 13959-02-9 3-bromoisonicotinic acid 
• 13959-01-8 ethyl 3-bromopyridine-4-carboxylate 

Downstream Products

• 1423014-73-6 ethyl 1-methyl-3-phenyl-1,2,5,6-tetrahydropyridine-4-carboxylate 
• 1423014-74-7 C₂₃H₂₇NO₄ 
• 1423014-75-8 C₂₃H₂₅NO₃ 
• 1423014-72-5 C₁₅H₁₆NO₂⁽¹⁺⁾*I^(1-) 
• 104096-15-3 3-phenylpyridine-4-carboxylic acid 

Relevant articles and documents

INHIBITORS OF FIBROBLAST ACTIVATION PROTEIN

Compounds and compositions for modulating fibroblast activation protein (FAP) are described. The compounds and compositions may find use as therapeutic agents for the treatment of diseases, including hyperproliferative diseases.

Direct arylation of substituted pyridines with arylboronic acids catalyzed by iron(II) oxalate

The direct arylation of substituted pyridines with several arylboronic acids has been developed. This transformation could proceed readily at ambient temperature using inexpensive reagents: iron(II) oxalate as a catalyst, potassium persulfate as a co-oxidant, which can afford the arylated products in mild to good yields. The mechanism is presumed to proceed through a nucleophilic radical addition to the pyridines with in situ reoxidation.