618383-47-4 Usage
General Description
3-(4-Methoxyphenyl)-5-isoxazolecarboxylic acid is a chemical compound with the molecular formula C11H9NO4. It is a heterocyclic compound that contains an isoxazole ring and a carboxylic acid group. 3-(4-METHOXYPHENYL)-5-ISOXAZOLECARBOXYLIC ACID can be used as a building block in organic synthesis for the creation of pharmaceuticals, agrochemicals, and other fine chemicals. It has potential applications in medicinal chemistry and drug discovery due to its ability to modulate molecular targets in various biological pathways. Its unique structure and functional groups make it a versatile compound for the development of new drugs and biologically active molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 618383-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,8,3,8 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 618383-47:
(8*6)+(7*1)+(6*8)+(5*3)+(4*8)+(3*3)+(2*4)+(1*7)=174
174 % 10 = 4
So 618383-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO4/c1-15-8-4-2-7(3-5-8)9-6-10(11(13)14)16-12-9/h2-6H,1H3,(H,13,14)
618383-47-4Relevant articles and documents
Synthesis, cytotoxic activity and binding model analysis of novel isoxazole-docetaxel analogues with C3′-N modification
Chen, Ming,Liu, Jiyuan,Tian, Zhen,Liu, Xueying,Zhang, Shengyong
, p. 1355 - 1365 (2018/04/10)
Structure–activity relationship (SAR) studies confirm that modifications at C-3′ position can lead to the development of highly potent novel taxoids. We designed and synthesized a series of novel isoxazole-docetaxel analogues A1–A5 by introducing isoxazol
One-pot copper(I)-catalyzed synthesis of 3,5-disubstituted isoxazoles
Hansen, Trond V.,Wu, Peng,Fokin, Valery V.
, p. 7761 - 7764 (2007/10/03)
3,5-Disubstituted isoxazoles are obtained in good yields by a convenient one-pot, three-step procedure utilizing a regioselective copper(I)-catalyzed cycloaddition reaction between in situ generated nitrile oxides and terminal acetylenes. Most functional
