CAS 71205-17-9

(E)-METHYL 3-(4-BROMOPHENYL)ACRYLATE

Description:

(E)-Methyl 3-(4-bromophenyl)acrylate is an organic compound characterized by its acrylate structure, which features a double bond between the carbon atoms in the acrylate moiety. The presence of the 4-bromophenyl group indicates that a bromine atom is substituted on the phenyl ring, which can influence the compound's reactivity and physical properties. This compound typically appears as a colorless to pale yellow liquid and has a distinctive aromatic odor. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water due to its hydrophobic nature. The compound is often used in organic synthesis and polymer chemistry, particularly in the production of specialty polymers and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Safety precautions should be observed when handling this compound, as it may pose health risks, including skin and eye irritation. Proper storage in a cool, dry place away from light is recommended to maintain its stability.

Synonyms:

• Specs Ab-131/40027014
• Methyl (E)-3-(4-Bromophenyl)-2-Propenoate

(E)-Methyl 3-(4-bromophenyl)acrylate

CAS: 71205-17-9

Formula: C₁₀H₉BrO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 241.0813

Ref: IN-DA00FD2S

Methyl trans-4-bromocinnamate

CAS: 71205-17-9

Methyl trans-4-bromocinnamate

Formula: C₁₀H₉BrO₂

Purity: 98%

Color and Shape: white solid

Molecular weight: 241.08g/mol

Ref: 54-OR15501

Methyl (E)-3-(4-bromophenyl)acrylate

CAS: 71205-17-9

Purity: 98%

Molecular weight: 241.0839996

Ref: 10-F693472

(E)-Methyl 3-(4-bromophenyl)acrylate

CAS: 71205-17-9

(E)-Methyl 3-(4-bromophenyl)acrylate is an isoenzyme that belongs to the group of cinnamic acid derivatives. It has been shown to induce apoptotic cell death in human ovarian carcinoma cells. This compound inhibits the production of histones and DNA, which may lead to the inhibition of transcription and replication of mRNA. (E)-Methyl 3-(4-bromophenyl)acrylate also induces modifications in proteins, such as acetylation, which may account for its apoptotic effects. Research has shown that (E)-methyl 3-(4-bromophenyl)acrylate has equitoxic effects on aryl halides and aryl chlorides.

Formula: C₁₀H₉BrO₂

Purity: Min. 95%

Molecular weight: 241.08 g/mol

Ref: 3D-WCA20517