7782-21-0

Basic information

• Product Name: (RS)-2-phenylpentanoic acid
• Synonyms: (RS)-2-phenylpentanoic acid
• CAS NO: 7782-21-0
• Molecular Weight: 178.231
• Mol File: 7782-21-0.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: (RS)-2-phenylpentanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (RS)-2-phenylpentanoic acid(7782-21-0)
• EPA Substance Registry System: (RS)-2-phenylpentanoic acid(7782-21-0)

Safety Data

• Hazardous Substances Data: 7782-21-0(Hazardous Substances Data)

Upstream product

• 5153-67-3 nitrostyrene 
• 927-77-5 n-propylmagnesium bromide 
• 103-82-2 phenylacetic acid 
• 107-08-4 1-iodo-propane 
• 124-38-9 carbon dioxide 
• 104-51-8 1-butylbenzene 
• 51090-00-7 N,N-dimethyl-1-phenylbutan-1-amine 
• 100-42-5 styrene 
• 2386-64-3 ethylmagnesium chloride 
• 106-94-5 propyl bromide 
• 88223-42-1 ethyl 2-phenylpentanoate 
• 71285-08-0 3,4,4,5,5-Pentachlor-2-phenyl-2-cyclopenten-1-on 
• 140-29-4 phenylacetonitrile 
• 101-41-7 benzeneacetic acid methyl ester 

Downstream Products

• 86-41-9 2-phenyl-valeric acid-(2-diethylamino-ethyl ester) 
• 1228456-31-2 p-nitrophenyl 2-phenylpentanoate 
• 35010-24-3 2-phenyl-pentanoic acid methyl ester 
• 19031-71-1 (1-fluorobutyl)benzene 
• 1016391-49-3 2-phenyl-N-(2-(pyrrolidin-1-yl)phenyl)pentanamide 
• 1327338-03-3 C₁₁H₁₃⁽²⁾HO₂ 
• 1217298-31-1 C₁₀H₁₅OP*C₁₁H₁₄O₂ 
• 7782-25-4 (S)-(+)-2-phenylvaleric acid 
• 7782-27-6 (R)-2-phenylpentanoic acid 
• 1034110-31-0 (R,S)-N-(tert-butyloxycarbonyl)-α-n-propylbenzylamine 
• 40628-82-8 (+/-)-acetic acid-(2-phenyl-pentyl ester) 
• 495-40-9 propiophenone 
• 3578-16-3 2-phenyl-valeric acid-(3-diethylamino-propyl ester) 
• 40327-98-8 (+/-)-2-phenyl-valeric acid-chloride 

Relevant articles and documents

Direct competitive enzyme-linked immunosorbent assay for the determination of the highly polar short-chain sulfophenyl carboxylates

A direct enzyme-linked immunosorbent assay for the detection of the short-chain sulfophenylcarboxylic acids (SPCs), the main metabolites of the linear alkylbenzene-sulfonates, is reported. Six SPCs (2C3, 2C 4, 3C4, 2C

Photocarboxylation of Benzylic C-H Bonds

The carboxylation of sp3-hybridized C-H bonds with CO2 is a challenging transformation. Herein, we report a visible-light-mediated carboxylation of benzylic C-H bonds with CO2 into 2-arylpropionic acids under metal-free conditions. Photo-oxidized triisopropylsilanethiol was used as the hydrogen atom transfer catalyst to afford a benzylic radical that accepts an electron from the reduced form of 2,3,4,6-tetra(9H-carbazol-9-yl)-5-(1-phenylethyl)benzonitrile generated in situ. The resulting benzylic carbanion reacts with CO2 to generate the corresponding carboxylic acid after protonation. The reaction proceeded without the addition of any sacrificial electron donor, electron acceptor or stoichiometric additives. Moderate to good yields of the desired products were obtained in a broad substrate scope. Several drugs were successfully synthesized using the novel strategy.

Zirconocene-catalyzed sequential ethylcarboxylation of alkenes using ethylmagnesium chloride and carbon dioxide

The zirconocene-catalyzed sequential ethylcarboxylation of alkenes using ethylmagnesium chloride and carbon dioxide has been developed. A range of alkenes were transformed into the corresponding carboxylic acids in high yields.