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2-Propenoic acid, 3-(3,4-dichlorophenyl)-3-(4-propoxyphenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133263-53-3

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133263-53-3 Usage

General Description

The chemical "2-Propenoic acid, 3-(3,4-dichlorophenyl)-3-(4-propoxyphenyl)-, (Z)-" is a compound with the molecular formula C18H14Cl2O3. It is a derivative of acrylic acid and contains two aromatic rings with chlorine and propoxy substituents. The compound is categorized as a carboxylic acid and is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. The (Z)- stereochemistry indicates that the substituents on the double bond are oriented in a cis configuration, impacting the compound's reactivity and biological activity. This chemical is utilized in various industries and research fields due to its versatile properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 133263-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,2,6 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133263-53:
(8*1)+(7*3)+(6*3)+(5*2)+(4*6)+(3*3)+(2*5)+(1*3)=103
103 % 10 = 3
So 133263-53-3 is a valid CAS Registry Number.

133263-53-3Upstream product

133263-53-3Relevant academic research and scientific papers

N-ACRYLOYLPIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS PAF ANTAGONISTS

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, (2008/06/13)

Compounds of formula (I): STR1 wherein R 1 and R 2 is each--R 5,--CH=CH--R 5 or--C C--R 5, wherein R. sup.5 is optionally substituted aryl or aromatic heterocyclic; R 3 is hydrogen, alkyl, cyano or--R 5 ; X is oxygen or sulfur; A is 1,4-piperazin-1, 4-diyl or a 1,4-homopiperazin-1,4-diyl; B' is alkylene, carbonyl, thiocarbonyl, sulfinyl or sulfonyl; and R 4 is optionally substituted phenyl and pharmaceutically acceptable salts thereof have valuable PAF antagonist activity, and may be prepared by reacting a compound containing the piperazine or homopiperazine part of the molecular with a compound containing the other part of the molecule.

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