20432-24-0 Usage
Description
(2Z)-2-(4-nitrophenyl)-3-phenylprop-2-enoic acid, also known as trans-4-(4-nitrophenyl)-3-phenylbut-2-enoic acid, is a chemical compound with the molecular formula C15H11NO4. It belongs to the class of organic compounds known as nitrobenzenes. (2Z)-2-(4-nitrophenyl)-3-phenylprop-2-enoic acid has a trans-geometry around the C=C double bond and features a phenyl group at both the second and third positions. It is characterized by its potential for photochemical reactions and its use in various industrial and scientific applications.
Uses
Used in Dye Intermediates:
(2Z)-2-(4-nitrophenyl)-3-phenylprop-2-enoic acid is used as a key intermediate for the production of dyes, due to its chemical structure that can be further modified to create a range of colored compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (2Z)-2-(4-nitrophenyl)-3-phenylprop-2-enoic acid is used as a building block for the synthesis of various drugs. Its unique structure allows for the development of new medicinal compounds with potential therapeutic properties.
Used in Organic Synthesis:
(2Z)-2-(4-nitrophenyl)-3-phenylprop-2-enoic acid is also utilized in organic synthesis for creating a variety of organic molecules. Its reactivity and structural features make it a valuable component in the synthesis of complex organic compounds.
Used in Photochemistry:
(2Z)-2-(4-nitrophenyl)-3-phenylprop-2-enoic acid has potential applications in the field of photochemistry. It can undergo photochemical reactions with other compounds, making it a candidate for research and development in areas such as photoactive materials and chemical sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 20432-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,3 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20432-24:
(7*2)+(6*0)+(5*4)+(4*3)+(3*2)+(2*2)+(1*4)=60
60 % 10 = 0
So 20432-24-0 is a valid CAS Registry Number.
20432-24-0Relevant articles and documents
Carboxylation of styrenes with CBr4 and DMSO via cooperative photoredox and cobalt catalysis
Song, Cai-Xia,Chen, Ping,Tang, Yu
, p. 11233 - 11243 (2017/02/26)
Cooperative photoredox and cobalt catalyzed carboxylation of styrenes with CBr4 to afford the corresponding α,β-unsaturated carboxylic acids has been realized through radical addition and Kornblum (DMSO) oxidation. DMSO serves as the oxidant, oxygen source and solvent under these photocatalytic conditions.
Substituent position-driven reaction pathways in the heterogeneous one-pot reduction/asymmetric hydrogenation of nitro-substituted (E)-2,3- diphenylpropenoic acids over Pd catalyst
Szoelloesi, Gyoergy,Bartok, Mihaly
experimental part, p. 16 - 27 (2012/03/11)
The reaction pathway in the heterogeneous enantioselective hydrogenation of nitro-substituted (E)-2,3-diphenylpropenoic acids over Pd catalyst modified by cinchonidine is determined by the position of the substituent. The reaction route was indicated by the H2 consumption curve and enantioselectivity of the final amino acid or 3-phenyl-1,2,3,4-tetrahydro-2- quinolone formed by intramolecular amidation. The obtained enantioselectivities were low with the exception of acids bearing nitro substituent in para position on the 3-phenyl moiety, the latter resulting in good, up to 80 % optical purity. The present study is the first to report the enantioselective heterogeneous catalytic preparation of 1,2,3,4-tetrahydro-2-quinolones and presents an attractive method for obtaining optically enriched 3-(4-aminophenyl)-2- phenylpropionic acids. ARKAT-USA, Inc.
Spasmolytics. II. 3-Tropanyl 2,3-diarylacrylates.
Caldwell,Finkelstein,Goldman,Sivak,Schlosser,Pelikan,Groves
, p. 1076 - 1079 (2007/10/07)
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