15121-71-8

Basic information

• Product Name: (E)-2-methyl-3-benzoylpropenoic acid
• Synonyms: (E)-2-methyl-3-benzoylpropenoic acid
• CAS NO: 15121-71-8
• Molecular Weight: 190.199
• Mol File: 15121-71-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-2-methyl-3-benzoylpropenoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-methyl-3-benzoylpropenoic acid(15121-71-8)
• EPA Substance Registry System: (E)-2-methyl-3-benzoylpropenoic acid(15121-71-8)

Safety Data

• Hazardous Substances Data: 15121-71-8(Hazardous Substances Data)

Upstream product

• 15732-75-9 3-benzoyl-2-methylenepropionic acid 
• 91909-83-0 (E)-ethyl 2-methyl-4-oxo-4-phenylbut-2-enoate 
• 7647-01-0 hydrogenchloride 
• 101105-99-1 2-methyl-2-morpholino-4-oxo-4-phenyl-butyric acid 
• 15732-77-1 methyl (E)-2-methyl-4-oxo-4-phenylbut-2-enoate 
• 93-58-3 benzoic acid methyl ester 
• 1015-28-7 dimethyl (2-oxo-2-phenylethyl)phosphonate 
• 71-43-2 benzene 
• 2170-03-8 itaconic acid anhydride 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 

Downstream Products

• 1771-65-9 2-methyl-4-oxo-4-phenylbutanoic acid 
• 336624-91-0 2-methyl-4-oxo-4-phenyl-cis-crotonic acid 
• 15732-78-2 trans-2-Benzoyl-1-methyl-cyclopropan-⁽¹⁾-methylester 
• 84143-18-0 (S)-2-Methyl-4-oxo-4-phenylbutanoic acid 
• 84143-17-9 (R)-2-methyl-4-oxo-4-phenylbutanoic acid 
• 1590-06-3 (+/-)-<2-Methyl-2-oxo-1.2.3.4-tetrahydro-2-naphthyl>-essigsaeure 
• 1590-05-2 (+/-)-3-Carboxy-3-methyl-5-phenyl-valeriansaeure 
• 101670-82-0 2-chloro-2-methyl-3-benzoylpropionic acid 
• 1589-98-6 (+/-)-γ-Benzoyl-β-carboxy-β-methyl-buttersaeure 
• 15732-77-1 methyl (E)-2-methyl-4-oxo-4-phenylbut-2-enoate 
• 101105-99-1 2-methyl-2-morpholino-4-oxo-4-phenyl-butyric acid 

Relevant articles and documents

Highly Chemo- And Enantioselective Hydrogenation of 2-Substituted-4-oxo-2-alkenoic Acids

The highly chemo- and enantioselective hydrogenation of (E)-2-substituted-4-oxo-2-alkenoic acids was established for the first time using the Rh/JosiPhos complex, affording a series of chiral α-substituted-γ-keto acids with excellent results (up to 99% yield and >99% ee) and high efficiency (up to 3000 TON). In addition, the importance of this methodology was further demonstrated by a concise and gram-scale synthesis of the anti-inflammatory drug (R)-flobufen.