132434-55-0 Usage
Description
(2E)-3-furan-2-yl-1-(3-nitrophenyl)prop-2-en-1-one is a chemical compound with the molecular formula C11H7NO4. It is a yellow crystalline solid that features a furan ring, a nitrophenyl group, and a prop-2-en-1-one moiety. (2E)-3-furan-2-yl-1-(3-nitrophenyl)prop-2-en-1-one is commonly used as a reactant in organic synthesis for the production of other compounds and serves as a starting material in the pharmaceutical industry for the synthesis of various drugs.
Uses
Used in Organic Synthesis:
(2E)-3-furan-2-yl-1-(3-nitrophenyl)prop-2-en-1-one is used as a reactant in organic synthesis for the creation of other compounds. Its unique molecular structure, which includes a furan ring and a nitrophenyl group, makes it suitable for a variety of chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2E)-3-furan-2-yl-1-(3-nitrophenyl)prop-2-en-1-one is used as a starting material for the synthesis of various drugs. Its structural components allow for the development of new medicinal compounds with potential therapeutic applications.
Safety Measures:
It is important to handle (2E)-3-furan-2-yl-1-(3-nitrophenyl)prop-2-en-1-one with proper safety measures due to its potential hazards. As with any chemical compound, appropriate precautions should be taken to minimize risks during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 132434-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,3 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132434-55:
(8*1)+(7*3)+(6*2)+(5*4)+(4*3)+(3*4)+(2*5)+(1*5)=100
100 % 10 = 0
So 132434-55-0 is a valid CAS Registry Number.
132434-55-0Relevant articles and documents
Studies of NMR Chemical Shifts of Chalcone Derivatives of Five-membered Monoheterocycles and Determination of Aromaticity Indices
Jeong, Eun Jeong,Lee, In-Sook Han
, p. 668 - 673 (2019/07/12)
A series of the chalcone derivatives of the five-membered monoheterocyclic compounds, (E)-1-aryl-3-heteroarylpropen-1-ones, were prepared by aldol condensation of the corresponding aldehydes of thiophene, pyrrole, and furan with m- and p-substituted acetophenones. Similar condensation of the acetyl compounds of the heterocycles with m- and p-substituted benzaldehydes gave another series of the chalcone derivatives, (E)-1-heteroaryl-3-arylpropen-1-ones. The 13C chemical shift values (δC) of the chalcone derivatives were determined in order to find if they correlated with the Hammett σ values. A good correlation, especially for the β-C for both series, was found for the 13C chemical shift values (δC) of the chalcone derivatives with the Hammett σ values. The chemical shift values of the β-C of the heterocyclic compounds were plotted against those of the benzene derivatives. The resulting slopes were found to be close to the values of the aromaticity indices.
Ultrasound promoted synthesis of α,α'-bis(substituted furfurylidene) cycloalkanones and chalcones
Li, Ji-Tai,Chen, Guo-Feng,Wang, Jian-Xin,Li, Tong-Shuang
, p. 965 - 971 (2007/10/03)
Condensation of furfural with cycloalkanones and substituted acetophenones catalysed by potassium hydroxide results α,α'- bis(substituted furfurylidene) cycloalkanones and chalcones in high yield under ultrasound irradiation in 4-50 min.