137013-00-4 Usage
Description
(2E)-3-(3,4-DIETHOXYPHENYL)ACRYLIC ACID is a chemical compound with the molecular formula C14H16O4. It is a derivative of acrylic acid, featuring a phenyl group with two ethoxy (C2H5O) groups attached. (2E)-3-(3,4-DIETHOXYPHENYL)ACRYLIC ACID is characterized by its unique structure and properties, which make it a versatile molecule for various applications in organic synthesis, pharmaceutical research, and materials science.
Uses
Used in Organic Synthesis:
(2E)-3-(3,4-DIETHOXYPHENYL)ACRYLIC ACID is used as a building block in organic synthesis for the creation of new compounds with specific properties. Its reactivity and functional groups allow chemists to modify and incorporate it into more complex molecules, leading to the development of novel chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2E)-3-(3,4-DIETHOXYPHENYL)ACRYLIC ACID is used as a starting material or intermediate in the synthesis of new drug candidates. Its structure and properties make it suitable for investigating its interactions with biological targets, such as enzymes or receptors. This allows researchers to design new compounds with improved pharmacological properties and potential therapeutic applications.
Used in Materials Science:
(2E)-3-(3,4-DIETHOXYPHENYL)ACRYLIC ACID may have potential uses in materials science, particularly in the development of new polymers or coatings. Its unique structure and properties could contribute to the creation of innovative materials with specific characteristics, such as improved durability, stability, or functionality.
Overall, (2E)-3-(3,4-DIETHOXYPHENYL)ACRYLIC ACID is a versatile compound with a wide range of applications across different industries, including organic synthesis, pharmaceutical research, and materials science. Its unique structure and properties make it a valuable molecule for the development of new compounds and materials with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 137013-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,1 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137013-00:
(8*1)+(7*3)+(6*7)+(5*0)+(4*1)+(3*3)+(2*0)+(1*0)=84
84 % 10 = 4
So 137013-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O4/c1-3-16-11-7-5-10(6-8-13(14)15)9-12(11)17-4-2/h5-9H,3-4H2,1-2H3,(H,14,15)/b8-6+
137013-00-4Relevant articles and documents
Synthesis, crystal structure, Hirshfeld surfaces analysis and anti-ischemic activity of cinnamide derivatives
Zhong, Jian-gang,Han, Jia-pei,Li, Xiao-feng,Xu, Yi,Zhong, Yan,Wu, Bin
, p. 72 - 78 (2018)
Two cinnamide derivatives, namely, (E)-1-(4-(bis(4-methylphenyl)- methyl)piperazin-1-yl)-3-(3,4-diethoxyphenyl)prop-2-en-1-one (5) and (E)-1-(4-(bis- (4-fluorophenyl)methyl)piperazin-1-yl)-3-(4-methoxyphenyl)prop-2-en-1-one (6), have been synthesized and characterized by IR spectra, High resolution mass spectra, 1H NMR spectra, 13C NMR spectra. The compound 5 is a novel compound and has never been reported in the literature. Their crystal structures were studied by single-crystal X-ray diffraction. They all crystallize in the monoclinic system. The single-crystal X-ray revealed that compound 5 has infinite X-shaped 1-D polymeric chains structure and compound 6 has a layered 3-D structure by intermolecular interactions. Hirshfeld surface analysis demonstrated the presence of H?H, O?H, C?H, F?H, C[sbnd]H?π and π?π intermolecular interactions. In addition, the MTT assay results indicated that the compounds 5 and 6 display effective activities against neurotoxicity which is induced by glutamine in PC12 cells. The in vivo experiment indicated that the compound 6 has a good protective effect on cerebral infarction.
