261527-26-8

Basic information

• Product Name: 1-hydroxy-4-methyl-1-(4-nitrophenyl)pentan-3-one
• Synonyms: 1-hydroxy-4-methyl-1-(4-nitrophenyl)pentan-3-one
• CAS NO: 261527-26-8
• Molecular Weight: 237.255
• Mol File: 261527-26-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-hydroxy-4-methyl-1-(4-nitrophenyl)pentan-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-hydroxy-4-methyl-1-(4-nitrophenyl)pentan-3-one(261527-26-8)
• EPA Substance Registry System: 1-hydroxy-4-methyl-1-(4-nitrophenyl)pentan-3-one(261527-26-8)

Safety Data

• Hazardous Substances Data: 261527-26-8(Hazardous Substances Data)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 7152-15-0 ethyl 4-methyl-3-oxo-pentanoate 
• 5650-76-0 isobutyrylacetic acid 

Downstream Products

• 86983-92-8 (E)-4-methyl-1-(p-nitrophenyl)-1-penten-3-one 
• 261527-36-0 3-[2-(p-aminophenyl)-ethyl]-3-hydroxy-4-methylpentanoic acid 
• 313256-73-4 3-hydroxy-3-isopropyl-5-(p-nitrophenyl)-4-pentenoic acid benzyl ester 
• 261527-25-7 3-[2-(p-N-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid 
• 261527-27-9 1-acetoxy-4-methyl-1-(p-nitrophenyl)pentan-3-one 

Relevant articles and documents

Lipase-catalysed decarboxylative aldol reaction and decarboxylative Knoevenagel reaction

Acrylic resin immobilized Candida antarctica lipase B (CAL-B) is able to catalyse decarboxylative aldol reaction and decarboxylative Knoevenagel reaction with good to excellent yields.

Application of the Sch?pf method to optimization of the synthesis of 3-[2-(p-N-acetylaminophenyl)ethyl]-3-hydroxy-4-methylpentanoic acid: Simultaneous reduction of three functional groups to maximize yield and throughput

Application of the Sch?pf method to development of a high yield condensation process to prepare a labile β-(p-nitrophenyl)-α,β-unsaturated ketone system, along with development of a procedure for simultaneous hydrogenation/hydrogenolysis of olefin, benzyl