CAS 940-61-4
:2-Propenoic acid, 3-(4-methylphenyl)-, (E)-
Description:
2-Propenoic acid, 3-(4-methylphenyl)-, (E)-, also known as 4-methylphenyl acrylate, is an organic compound characterized by its acrylate structure, which features a vinyl group and a carboxylic acid functional group. This compound is typically a colorless to pale yellow liquid with a characteristic odor. It is soluble in organic solvents and exhibits limited solubility in water. The (E)- configuration indicates that the substituents around the double bond are on opposite sides, which can influence its reactivity and physical properties. 2-Propenoic acid, 3-(4-methylphenyl)- is used in various applications, including as a monomer in polymer synthesis, particularly in the production of coatings, adhesives, and plastics. Its reactivity allows it to participate in polymerization reactions, making it valuable in the development of materials with specific mechanical and thermal properties. Additionally, it may have applications in the field of organic synthesis and as an intermediate in the manufacture of other chemical compounds. Safety precautions should be taken when handling this substance, as it can be irritating to the skin and eyes.
Formula:C10H10O2
Synonyms:- (2E)-3-(4-methylphenyl)acrylic acid(SALTDATA: FREE) USP/EP/BP
- -
- (2E)-3-(4-Methylphenyl)acrylicaci
- -Methylcinnamic acid
- p
- (2E)-3-(4-methylphenyl)acrylic acid(SALTDATA: FREE)
- trans
- 2-Propenoic acid, 3-(4-Methylphenyl)-, (E)-
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Found 4 products.
(2E)-3-(4-methylphenyl)acrylic acid
CAS:Formula:C10H10O2Purity:98%Color and Shape:SolidMolecular weight:162.1852(2E)-3-(4-methylphenyl)acrylic acid
CAS:(2E)-3-(4-methylphenyl)acrylic acidPurity:98%Molecular weight:162.19g/mol(E)-3-(4-Methylphenyl)-2-propenoic acid
CAS:<p>(E)-3-(4-Methylphenyl)-2-propenoic acid is a chlorinated cinnamic acid derivative that inhibits the formation of (E)-3-(4-methylphenyl)-2-propenoic acid. The rate of formation of (E)-3-(4-methylphenyl)-2-propenoic acid is inhibited by the presence of phosphorus pentachloride. It is also possible to synthesize 4-hydroxycinnamic acid, which has a similar inhibitory effect on the formation of (E)-3-(4-methylphenyl)-2-propenoic acid. This inhibition may be due to the polarizability and molecule size of (E)-3-(4-methylphenyl)-2-propenoic acid. The chloride ion can also affect this reaction through hydrogen bonding interactions with the fatty acids in (E)-3-(4-methylphenyl)-2-propenoic</p>Formula:C10H10O2Purity:Min. 95%Molecular weight:162.19 g/mol




