7315-68-6

Basic information

• Product Name: β-Methylbenzenebutyric acid
• Synonyms: 3-Methyl-4-phenylbutanoic acid;3-Methyl-4-phenylbutyric acid;β-Benzyl-β-methylpropionic acid;β-Methylbenzenebutanoic acid;3-methyl-4-phenylbutanoic acid3-methyl-4-phenylbutanoic acid
• CAS NO: 7315-68-6
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.2277
• Mol File: 7315-68-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 298.3°Cat760mmHg
• Flash Point: 195.4°C
• Appearance: /
• Density: 1.068g/cm³
• Vapor Pressure: 0.000574mmHg at 25°C
• Refractive Index: 1.526
• CAS DataBase Reference: β-Methylbenzenebutyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: β-Methylbenzenebutyric acid(7315-68-6)
• EPA Substance Registry System: β-Methylbenzenebutyric acid(7315-68-6)

Safety Data

• Hazardous Substances Data: 7315-68-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H14O2/c1-9(8-11(12)13)7-10-5-3-2-4-6-10/h2-6,9H,7-8H2,1H3,(H,12,13)

Upstream product

• 6052-53-5 3-Methyl-4-phenyl-3-butensaeure 
• 7315-67-5 3-methyl-4-oxo-4-phenylbutanoic acid 
• 7148-59-6 2-cyano-3-methyl-4-phenyl-crotonic acid ethyl ester 
• 93-55-0 1-phenyl-propan-1-one 
• 53852-50-9 3-methyl-4-phenylbut-2-enenitrile 
• 103-79-7 1-phenyl-acetone 
• 451-40-1 phenyl benzyl ketone 
• 64-18-6 formic acid 
• 3290-53-7 2-methyl-1-phenyl-2-propene 
• 78167-61-0 (2-methylpent-4-en-1-yl)benzene 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 7315-66-4 diethyl 2-(1-oxo-1-phenylpropan-2-yl)malonate 
• 52240-29-6 (1-methyl-2-oxo-2-phenyl-ethyl)-malonic acid 
• 68996-14-5 1-phenyl-2-methyl-3-bromopropane 

Downstream Products

• 138816-37-2 trans-4-methyl-5-phenylpyrrolidin-2-one 
• 7315-70-0 6-Benzyl-2-methyl-heptanon-⁽⁴⁾ 
• 7315-71-1 6-Benzyl-2-methyl-heptanol-⁽⁴⁾ 
• 13615-40-2 3-methylnaphthalen-1-ol 
• 85268-97-9 2,4-dimethyl-5-phenyl-2-pentanol 
• 85268-66-2 1,2,3,4-tetrahydro-1,1,3-trimethylnaphtalene 
• 20568-06-3 4,5-dihydro-4-methyl-5-phenyl-2(3H)-furanone 
• 69573-51-9 3-Methyl-4-phenylbutansaeure-methylester 
• 14944-23-1 3-methyl-1-tetralone 
• 7315-69-7 3-methyl-4-phenyl-butyryl chloride 
• 72277-22-6 3-Methyl-4-phenyl-butansaeure-ethylester 

Relevant articles and documents

An atom-economic approach to carboxylic acids via Pd-catalyzed direct addition of formic acid to olefins with acetic anhydride as a co-catalyst

An effective Pd-catalyzed hydrocarboxylation of olefins using formic acid with acetic anhydride as a co-catalyst is described. A variety of carboxylic acids are obtained in good yields with high regioselectivities under mild reaction conditions without the use of toxic CO gas.

NAPHT- 2 -YLACETIC ACID DERIVATIVES TO TREAT AIDS

The invention provides compounds of formula (I): or a salt thereof as described herein. The invention also provides pharmaceutical compositions comprising a compound of formula I, processes for preparing compounds of formula (I), intermediates useful for preparing compounds of formula I and therapeutic methods for treating the proliferation of the HIV virus, treating AIDS or delaying the onset of AIDS or ARC symptoms in a mammal using compounds of formula (I).

Synthese de methoxycarbonylindenes, dihydro-1,2 naphtalenes et benzocycloheptene. Obtention des indanones-1, des tetralones-1 et de la benzosuberone correspondantes

The synthesis of methoxycarbonylindenes, 1,2-dihydro-naphtalenes, and benzocycloheptene starting from the corresponding 1-indanones, 1-tetralones, and benzosuberone is reported.The starting ketones were synthesized by methods described in the literature which were optimized; in some cases new processes are described.