101458-36-0

Basic information

• Product Name: Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-Methyl-, ethyl e
• Synonyms: Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-Methyl-, ethyl e;Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-Methyl-, ethyl ester
• CAS NO: 101458-36-0
• Molecular Formula: C₁₂H₁₄Br₂O₂
• Molecular Weight: 350.04636
• Mol File: 101458-36-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-Methyl-, ethyl e(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-Methyl-, ethyl e(101458-36-0)
• EPA Substance Registry System: Benzenepropanoic acid, .alpha.,.beta.-dibroMo-4-Methyl-, ethyl e(101458-36-0)

Safety Data

• Hazardous Substances Data: 101458-36-0(Hazardous Substances Data)

Usage

General Description

Benzenepropanoic acid, .alpha.,.beta.-dibromo-4-methyl-, ethyl ester is a chemical compound that is derived from benzenepropanoic acid, also known as phenylpropanoic acid. The compound contains two bromine atoms attached to the 4-methyl group, and it is an ethyl ester, meaning it has an ethyl group attached to the carboxyl group of the acid. This chemical may have various applications in organic synthesis, pharmaceuticals, and the manufacture of specialty chemicals. It is important to handle this compound with care, as brominated compounds can be hazardous and should be used in a controlled environment by trained professionals.

Upstream product

• 20511-20-0 ethyl p-methylcinnamate 
• 108-88-3 toluene 
• 97585-04-1 ethyl (E)-3-(4-methylphenyl)acrylate 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 21053-25-8 5-p-tolyl-isoxazol-3-one 
• 100281-80-9 (4S,5S)-3-Benzyl-2-phenyl-5-p-tolyl-4,5-dihydro-3H-imidazole-4-carboxylic acid ethyl ester 
• 100281-80-9 (4S,5R)-3-Benzyl-2-phenyl-5-p-tolyl-4,5-dihydro-3H-imidazole-4-carboxylic acid ethyl ester 
• 83501-14-8 (E)-2-Bromo-3-p-tolyl-acrylic acid ethyl ester 
• 52188-06-4 ethyl 3-(4-methylphenyl)prop-2-ynoate 

Relevant articles and documents

NOVEL BENSOPHENONE DERIVATIVES OR SALTS THEREOF

A benzophenone derivative represented by the following formula: whereinR1 represents, for example, an optionally substituted heterocyclic group, or a substituted phenyl group; Z represents, for example, an alkylene group; R2 represents, for example, a carboxyl group optionally protected with alkyl;R3 represents, for example, an optionally protected hydroxyl group; R4 represents, for example, an optionally substituted cycloalkyloxy group; and R5 represents, for example, a hydrogen atom, ???or a salt thereof has anti-arthritic activity, inhibits bone destruction caused by arthritis, and provides high safety and excellent pharmacokinetics and thus is useful as therapeutic agent for arthritis. These compounds have inhibitory effect on AP-1 activity and are useful as preventive or therapeutic agent for diseases in which excessive expression of AP-1 is involved.

Transmission of substituent effects through extended systems-III. p-Substituted ethyl trans cinnamates and phenylpropiolates

Infrared data and 13C chemical shifts are reported for a series of ethyl p-substituted trans-cinnamates and ethyl phenylpropiolates.The i.r. values include intensities for the benzene, ethylene and carbonyl vibrations which allow an estimation of resonance effects.The relative importance of the various mechanisms of transmission of substituent effects are discussed and compared to those previously reported for p-substituted trans cinnamonitriles.It is shown that the carbon-carbon triple bond is less efficient in transmitting substituent effects than carbon-carbon double bonds.