7064-33-7 Usage
General Description
5-(3-Bromophenyl)isoxazole is a chemical compound with the molecular formula C9H6BrNO. It belongs to the class of isoxazole derivatives, which are heterocyclic compounds containing a five-membered ring with three carbon atoms, one oxygen atom, and one nitrogen atom. The compound is characterized by the presence of a bromine atom on the phenyl ring attached to the isoxazole structure. 5-(3-BROMOPHENYL)ISOXAZOLE has potential applications in medicinal chemistry and pharmaceutical research, as isoxazole derivatives have been investigated for their various biological activities, including antimicrobial, antifungal, and anti-inflammatory properties. The 5-(3-Bromophenyl)isoxazole compound may also serve as a valuable building block in the synthesis of other organic compounds for research and industrial purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 7064-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7064-33:
(6*7)+(5*0)+(4*6)+(3*4)+(2*3)+(1*3)=87
87 % 10 = 7
So 7064-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C31H38N4O4S2/c1-7-11-34-28(33-17-19(2)13-20(3)18-33)23(21(4)24(16-32)29(34)36)15-27-30(37)35(31(40)41-27)12-10-22-8-9-25(38-5)26(14-22)39-6/h8-9,14-15,19-20H,7,10-13,17-18H2,1-6H3
7064-33-7Relevant articles and documents
Harnessing Stereospecific Z-Enamides through Silver-Free Cp?Rh(III) Catalysis by Using Isoxazoles as Masked Electrophiles
Debbarma, Suvankar,Bera, Sourav Sekhar,Maji, Modhu Sudan
, p. 835 - 839 (2019/01/26)
The stereospecific synthesis of Z-enamides is described in this paper. For the first time, isoxazoles have been employed as electrophiles in C-H functionalization to afford thermodynamically less stable Z-enamides utilizing salicylaldehydes in an atom- and step-economic fashion. The stereochemistry of enamides might originate from the relative disposition of atoms present in isoxazole and the intramolecular hydrogen bonding. The reaction showed excellent scope as several structurally and electronically diverse salicylaldehydes and isoxazoles reacted efficiently.
Activity-Based Proteome Profiling Probes Based on Woodward's Reagent K with Distinct Target Selectivity
Qian, Yong,Schürmann, Marc,Janning, Petra,Hedberg, Christian,Waldmann, Herbert
, p. 7766 - 7771 (2016/07/07)
Woodward's reagent K (WRK) is a reactive heterocyclic compound that has been employed in protein chemistry to covalently and unspecifically label proteins at nucleophilic amino acids, notably at histidine and cysteine. We have developed a panel of WRK-der
