382636-47-7 Usage
Uses
Used in Pharmaceutical Industry:
(2E)-3-(7-methyl-4-oxo-4H-chromen-3-yl)prop-2-enoic acid is used as a pharmaceutical compound for its potential therapeutic properties. The specific reasons for its use in this industry would depend on the results of further experimental research and testing, which could reveal its efficacy in treating certain conditions or diseases.
Used in Organic Synthesis:
In the field of organic synthesis, (2E)-3-(7-methyl-4-oxo-4H-chromen-3-yl)prop-2-enoic acid may serve as a key intermediate or building block for the creation of more complex molecules. Its unique structure, including the propenoic acid and chromen-3-yl groups, could be leveraged to synthesize novel compounds with specific functions or properties.
Check Digit Verification of cas no
The CAS Registry Mumber 382636-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,2,6,3 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 382636-47:
(8*3)+(7*8)+(6*2)+(5*6)+(4*3)+(3*6)+(2*4)+(1*7)=167
167 % 10 = 7
So 382636-47-7 is a valid CAS Registry Number.
382636-47-7Relevant academic research and scientific papers
Joshi, Ratnadeep S.,Mandhane, Priyanka G.,Badadhe, Pravin V.,Gill, Charansingh H.
, p. 735 - 738 (2011)
We report a new environmentally-benign, convenient and facile methodology for the synthesis of new series of 3(4-oxo-4H-chromen-3-yl)acrylic acid hydrazides derivatives designed by exploring the molecular hybridization approach between isoniazide and 3(4-
Synthesis of Chromone-Containing Allylmorpholines through a Morita–Baylis–Hillman-Type Reaction
Chernov, Nikita M.,Shutov, Roman V.,Barygin, Oleg I.,Dron, Mikhail Y.,Starova, Galina L.,Kuz'mich, Nikolay N.,Yakovlev, Igor P.
supporting information, p. 6304 - 6313 (2018/11/10)
The first example of an unusual addition of chromone-substituted acrylic acid to enamines is described. The process shows high versatility concerning both enamines and chromones. The reaction is catalyzed by tertiary amines and is highly likely of Morita–