85274-59-5

Basic information

• Product Name: N-phenyl-2-(pyridin-2-yl)acetamide
• Synonyms: N-phenyl-2-(pyridin-2-yl)acetamide
• CAS NO: 85274-59-5
• Molecular Weight: 212.251
• Mol File: 85274-59-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-phenyl-2-(pyridin-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-2-(pyridin-2-yl)acetamide(85274-59-5)
• EPA Substance Registry System: N-phenyl-2-(pyridin-2-yl)acetamide(85274-59-5)

Safety Data

• Hazardous Substances Data: 85274-59-5(Hazardous Substances Data)

Upstream product

• 61890-12-8 1-phenyl-2-[2]pyridyl-ethanone-(E)-oxime 
• 1658-42-0 methyl 2-pyridylacetate 
• 62-53-3 aniline 
• 2739-98-2 ethyl 2-(pyridinyl-2)acetate 
• 60-29-7 diethyl ether 
• 10026-13-8 phosphorus pentachloride 
• 67-66-3 chloroform 
• 1620-53-7 1-phenyl-2-pyridin-2-ylethanone 
• 5451-39-8 2-(pyridine-2-yl)acetamide 
• 108-90-7 chlorobenzene 
• 16179-97-8 pyridin-2-yl acetic acid hydrochloride 

Downstream Products

• 1658-42-0 methyl 2-pyridylacetate 
• 13115-43-0 2-pyridineacetic acid 
• 2739-98-2 ethyl 2-(pyridinyl-2)acetate 
• 23692-08-2 piperidin-2-yl-acetic acid methyl ester 
• 39998-21-5 (1-methyl-1H-pyridin-2-ylidene)-acetic acid methyl ester 
• 154410-82-9 methyl 2-hydroxyimino-2-(pyridyl-2')acetate 
• 15937-81-2 1,3-bis(2-pyridyl)propane 
• 54401-82-0 4-oxo-3-pyridin-2-yl-4H-quinolizine-1-carboxylic acid ethyl ester 
• 489-54-3 (+/-)-(7ac,14at)-dodecahydro-7r,14c-methano-dipyrido[1,2-a;1',2'-e][1,5]diazocine-6,13-dione 
• 489-54-3 (+/-)-(7ac,14ac)-dodecahydro-7r,14c-methano-dipyrido[1,2-a;1',2'-e][1,5]diazocine-6,13-dione 
• 489-54-3 (+/-)-10,17-dioxo-β-isosparteine 

Relevant articles and documents

Synthesis of β-Hydroxy α-Amino Acids through Br?nsted Base-Catalyzed syn-Selective Direct Aldol Reaction of Schiff Bases of Glycine o-Nitroanilide

Here we report the highly enantio- and syn-selective synthesis of β-hydroxy α-amino acids from glycine imine derivatives under Br?nsted base (BB) catalysis. The key of this approach is the use of benzophenone-derived imine of glycine o-nitroanilide as a pronucleophile, where the o-nitroanilide framework provides an efficient hydrogen-bonding platform that accounts for nucleophile reactivity and diastereoselectivity.