33817-23-1

Basic information

• Product Name: (S)-2-cyclohexyl-2-phenylpropanoic acid
• Synonyms: (S)-2-cyclohexyl-2-phenylpropanoic acid
• CAS NO: 33817-23-1
• Molecular Weight: 232.323
• Mol File: 33817-23-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-cyclohexyl-2-phenylpropanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-cyclohexyl-2-phenylpropanoic acid(33817-23-1)
• EPA Substance Registry System: (S)-2-cyclohexyl-2-phenylpropanoic acid(33817-23-1)

Safety Data

• Hazardous Substances Data: 33817-23-1(Hazardous Substances Data)

Upstream product

• 4370-98-3 2-cyclohexyl-2-phenylpropanoic acid 
• 4420-58-0 2-cyclohexyl-2-phenylpropanenitrile 

Downstream Products

• 40412-60-0 (S)-3-Cyclohexyl-3-methyl-indan-1-one 
• 40412-65-5 (S)-2-cyclohexyl-2-phenylpropanal 
• 40412-61-1 (S)-1-cyclohexyl-1-methyl-2,3-dihydro-1H-indene 
• 40412-64-4 (S)-2-Cyclohexyl-2-phenyl-propan-1-ol 
• 33817-26-4 (S)-3-Cyclohexyl-3-phenyl-butan-2-one 
• 40412-59-7 (S)-3-Cyclohexyl-3-phenyl-butyric acid 

Relevant articles and documents

Bioinspired Metal-Free Formal Decarbonylation of α-Branched Aliphatic Aldehydes at Ambient Temperature

A sequence of a Baeyer–Villiger oxidation and a Lewis acid-promoted reduction of the resulting formate with Et3SiH enabled the metal-free formal decarbonylation of tertiary and secondary aliphatic aldehydes. The new methodology mimics the biosynthetic decarbonylation pathway through oxidative C?C bond cleavage rather than the C(O)?H bond activation known from conventional Tsuji–Wilkinson-type reactions. The substrate scope is complementary to existing transition-metal-catalyzed protocols.