594836-76-7

Basic information

• Product Name: (R)-3-phenoxy-3-phenylpropanoic acid
• Synonyms: (R)-3-phenoxy-3-phenylpropanoic acid
• CAS NO: 594836-76-7
• Molecular Weight: 242.274
• Mol File: 594836-76-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-3-phenoxy-3-phenylpropanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-phenoxy-3-phenylpropanoic acid(594836-76-7)
• EPA Substance Registry System: (R)-3-phenoxy-3-phenylpropanoic acid(594836-76-7)

Safety Data

• Hazardous Substances Data: 594836-76-7(Hazardous Substances Data)

Upstream product

• 33603-90-6 (2Z)-2-bromo-3-phenyl-2-propenal 
• 104-55-2 3-phenyl-propenal 
• 77889-98-6 (E)-3-phenoxy-3-phenylacrylaldehyde 
• 1079366-62-3 (R)-3-phenoxy-3-phenylpropan-1-ol 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 108-95-2 phenol 
• 1086229-55-1 (E)-ethyl 3-phenoxy-3-phenylacrylate 
• 85551-57-1 (R)-1-Phenylbut-3-en-1-ol 
• 594836-75-6 (R)-phenyl 1-phenyl-3-butenyl ether 

Downstream Products

• 41886-75-3 (2R,4R)-(-)-cis-4-hydroxyflavan 
• 487-26-3 (R)-flavanone 

Relevant articles and documents

One-pot sequential asymmetric hydrogenation of β-aryl-β-aryloxy acroleins

A one-pot sequential asymmetric hydrogenation of β-aryl-β-aryloxy acroleins has been realized for the preparation of chiral 3-aryl-3-aryloxy alcohols with excellent yields and good enantioselectivities. This methodology can be employed in new synthetic routes for the synthesis of fluoxetine, atomoxetine, and related analogues.

Asymmetric synthesis of 2-substituted chroman-4-ones using lipase-catalyzed kinetic resolutions

2-Methylchroman-4-one and 2-phenylchroman-4-one were synthesized in optically active form. Their chiral intermediates were obtained via lipase-catalyzed enantioselective reactions.