2939-13-1

Basic information

• Product Name: 3-methyl-5-phenylpentanoic acid
• Synonyms: 3-methyl-5-phenylpentanoic acid
• CAS NO: 2939-13-1
• Molecular Formula: C₁₂H₁₆O₂
• Molecular Weight: 192.25424
• Mol File: 2939-13-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-methyl-5-phenylpentanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-5-phenylpentanoic acid(2939-13-1)
• EPA Substance Registry System: 3-methyl-5-phenylpentanoic acid(2939-13-1)

Safety Data

• Hazardous Substances Data: 2939-13-1(Hazardous Substances Data)

Upstream product

• 4467-30-5 4-methyl-6-phenyl-2H-pyran-2-one 
• 72277-03-3 diethyl 1-trimethylsilyloxy-2-butenylphosphonate 
• 103-63-9 1-phenyl-2-bromoethane 
• 107-93-7 (E)-but-2-enoic acid 
• 17376-04-4 2-phenethyl iodide 
• 67753-90-6 9-phenethyl-9-bora-bicyclo[3.3.1]nonane 
• 1261270-07-8 3-methyl-1-(1-methyl-1H-imidazol-2-yl)-5-phenyl-1-pentanone 
• 100-42-5 styrene 
• 55053-55-9 ethyl 5-phenyl-3-methyl-2-pentanoate 
• 36805-43-3 ethyl (E)-3-methyl-5-phenylpent-2-enoate 
• 71-43-2 benzene 
• 4166-53-4 3-methylglutaric anhydride 
• 152419-46-0 β-Methyl-γ-oxo-δ-phenyl-valeriansaeure 
• 72681-05-1 (E/Z)-3-methyl-5-phenylpent-2-enoic acid 

Downstream Products

• 55053-55-9 ethyl 5-phenyl-3-methyl-2-pentanoate 
• 2840-62-2 3-methyl-5-phenyl-valeric acid anilide 
• 94914-09-7 β-Methyl-δ-phenyl-valeriansaeure-p-toluidid 

Relevant articles and documents

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Conjugate addition of a primary carbon radical to α,β-unsaturated carboxylic acids

Triethylborane in the presence of trace oxygen was employed simultaneously as a radical initiator and carboxyl protecting group to promote the conjugate radical addition of 2-phenethyl iodide to α,β- unsaturated carboxylic acids in good yields. (C) 2000 Elsevier Science Ltd.

Silyl Phosphites. XVIII. Versatile Utility of α-(Trimethylsilyloxy)-alkylphosphonates as Key Intermediates for Transformation of Aldehydes into Several Carbonyl Derivatives

Carbonyl addition compounds of diethyl trimethylsilyl phosphite (DTMSP) with aldehydes were converted, by treatment with lithium diisopropylamide (LDA) followed by the successive alkylation and alkaline hydrolysis, to carbonyl derivatives involving aldehydes, unsymmetrical ketones, β,γ-unsaturated ketones, and carboxylic acids. β-Substituted carboxylic esters and γ-substituted lactones were prepared by use of the carbonyl addition compounds of DTMSP with α,β-unsaturated aldehydes.