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2-Propenoic acid, 3-(3-ethoxyphenyl)-, methyl ester, (2E)- is a chemical compound with the molecular formula C12H14O4. It is an organic ester derived from 2-propenoic acid, also known as acrylic acid, and features a 3-ethoxyphenyl group attached to the third carbon. The (2E)- notation indicates that the molecule has a specific geometric isomerism, with the double bond between the first and second carbon atoms in the E configuration. 2-Propenoic acid, 3-(3-ethoxyphenyl)-, methyl ester, (2E)- is characterized by its ester functional group, which is formed by the reaction of the carboxylic acid group of 2-propenoic acid with methanol. It is used in various applications, such as in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, due to its unique structure and reactivity.

923955-23-1

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923955-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923955-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,9,5 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 923955-23:
(8*9)+(7*2)+(6*3)+(5*9)+(4*5)+(3*5)+(2*2)+(1*3)=191
191 % 10 = 1
So 923955-23-1 is a valid CAS Registry Number.

923955-23-1Relevant academic research and scientific papers

Templating photodimerization of trans-cinnamic acid esters with a water-soluble Pd nanocage

Karthikeyan,Ramamurthy

, p. 452 - 458 (2007/10/03)

A water-soluble octahedral Pd nanocage acting as a reaction vessel templates the photodimerization of substituted trans-cinnamic acid methyl esters in water. Irradiation of the host-guest complexes of trans-cinnamic acid methyl esters with the Pd nanocage resulted in selective formation of a syn head-head dimer in addition to the corresponding cis isomer. These results suggest that the guest molecules are preoriented in a selective fashion with the hydrophilic ester group facing water and the hydrophobic aryl group tucked within the cavity of the host. Such an orientation occurs at the hydrophobic-hydrophilic interface between the nanocage exterior and interior. Weak intermolecular C-H-π and π-π interactions between the host and the guest(s) are likely to be responsible for the lack of mobility of the reactant olefins during their short excited-state lifetime.

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