CAS 96426-60-7
:methyl (2E)-3-(4-fluorophenyl)prop-2-enoate
Description:
Methyl (2E)-3-(4-fluorophenyl)prop-2-enoate, with the CAS number 96426-60-7, is an organic compound characterized by its ester functional group and a conjugated double bond system. This compound features a methyl ester group attached to a prop-2-enoate backbone, which contributes to its reactivity and potential applications in organic synthesis. The presence of the 4-fluorophenyl substituent enhances its electronic properties, potentially influencing its reactivity and interactions in chemical reactions. Methyl (2E)-3-(4-fluorophenyl)prop-2-enoate is typically a colorless to pale yellow liquid, exhibiting moderate volatility and solubility in organic solvents. Its structure suggests potential applications in pharmaceuticals, agrochemicals, and materials science, particularly in the development of compounds with specific biological activities or as intermediates in synthetic pathways. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.
Formula:C10H9FO2
InChI:InChI=1/C10H9FO2/c1-13-10(12)7-4-8-2-5-9(11)6-3-8/h2-7H,1H3/b7-4+
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Methyl 4-fluorocinnamate, predominantly trans
CAS:Formula:C10H9FO2Purity:98%Color and Shape:SolidMolecular weight:180.1757Methyl 4-fluorocinnamate
CAS:Formula:C10H9FO2Purity:98%Color and Shape:Low Melting SolidMolecular weight:180.178



