4842-61-9

Basic information

• Product Name: (S)-(+)-4'-methoxy-3-phenylbutyric acid
• Synonyms: (S)-(+)-4'-methoxy-3-phenylbutyric acid
• CAS NO: 4842-61-9
• Molecular Weight: 194.23
• Mol File: 4842-61-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (S)-(+)-4'-methoxy-3-phenylbutyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-4'-methoxy-3-phenylbutyric acid(4842-61-9)
• EPA Substance Registry System: (S)-(+)-4'-methoxy-3-phenylbutyric acid(4842-61-9)

Safety Data

• Hazardous Substances Data: 4842-61-9(Hazardous Substances Data)

Upstream product

• 199006-83-2 (S,R)-(+)-N-(1-ethyl-2-hydroxy)ethyl-N-(2-fluorobenzyl)-3-(p-methoxyphenyl)butanamide 
• 61292-83-9 (+/-)-ethyl 3-(4-methoxyphenyl)butanoate 
• 18310-76-4 3-(4'-methoxyphenyl)butanoyl chloride 
• 6555-30-2 3-(4-methoxyphenyl)butyric acid 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 4842-51-7 (-)-angolensin-4-methyl ether 
• 4842-48-2 (αR)-angolensin 
• 151800-31-6 (3(3S),4R)-3-<3-(4'-Methoxyphenyl)butanoyl>-4-phenyl-2-oxazolidinone 

Downstream Products

• 128677-80-5 C₁₆H₂₂O₄ 
• 128677-82-7 (S)-3-[(2R,3R)-2-Azido-3-(4-methoxy-phenyl)-butyryl]-4-benzyl-oxazolidin-2-one 
• 128693-81-2 (3(3S),4S)-4-benzyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone 
• 128677-83-8 (2R,3R)-2-Azido-3-(4-methoxyphenyl)butyric acid 
• 132338-27-3 (2R,3R)-2-amino-3-(4-methoxyphenyl)butyric acid 
• 128573-10-4 erythro-D-(2R,3R)-β-Methyltyrosine 
• 128677-79-2 (S)-3-[4-(1-Phenyl-1H-tetrazol-5-yloxy)-phenyl]-butyric acid methyl ester 
• 128693-80-1 (S)-3-(4-Trifluoromethanesulfonyloxy-phenyl)-butyric acid methyl ester 
• 128677-78-1 (S)-3-(4-Hydroxy-phenyl)-butyric acid methyl ester 
• 1441-20-9 (R)-(-)-3-phenylbutyric acid methyl ester 
• 146137-36-2 (3(3S),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone 
• 6739-21-5 (S)-3-(4-Hydroxy-phenyl)-butyric acid 

Relevant articles and documents

Lipase catalysed kinetic resolutions of 3-aryl alkanoic acids

Hydrolase catalysed kinetic resolutions leading to a series of 3-aryl alkanoic acids (≥94% ee) are described. Hydrolysis of the ethyl esters with a series of hydrolases was undertaken to identify biocatalysts that yield the corresponding acids with excellent enantiopurity in each case. Steric and electronic effects on the efficiency and enantioselectivity of the biocatalytic transformation were also explored.

Synthese Asymetrique. 2. Additions Conjuguees Enantioselectives de Reactifs de Grignard a la Cinnamamide et la Crotonamide derivant du (R)-(-)-N-(2-Fluorobenzyl)-2-Aminobutan-1-ol. Determination de l'exces Diastereomerique au moyen de la RMN de 19F

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Efficient Method for the Total Asymmetric Synthesis of the Isomers of β-Methyltyrosine

α-Amino acids modified at the β-carbon atom can provide topographical constraints when incorporated into a peptide.Such modifications can modulate the physical, chemical, and biological properties of the compound.In order to properly evaluate the effect o