887-90-1 Usage
Uses
Used in Pharmaceutical Research:
5-Bromo-3-(4-chlorophenyl)-2,1-benzisoxazole is used as a research compound for its potential as an anticonvulsant and anxiolytic agent, due to its unique chemical structure and pharmacological properties.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 5-Bromo-3-(4-chlorophenyl)-2,1-benzisoxazole is used as an active compound to explore its ability to combat various microorganisms, leveraging its chemical properties to inhibit microbial growth.
Used in Anticancer Applications:
5-Bromo-3-(4-chlorophenyl)-2,1-benzisoxazole is utilized as a candidate molecule in anticancer drug development, given its potential to target and affect cancer cells, based on its pharmacological profile and the presence of halogen atoms that may enhance its reactivity and binding affinity to biological targets.
Used in Medicinal Chemistry:
In medicinal chemistry, 5-Bromo-3-(4-chlorophenyl)-2,1-benzisoxazole serves as a key intermediate in the synthesis of various drug molecules, taking advantage of its structural features to create new compounds with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 887-90-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 887-90:
(5*8)+(4*8)+(3*7)+(2*9)+(1*0)=111
111 % 10 = 1
So 887-90-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H7BrClNO/c14-9-3-6-12-11(7-9)13(17-16-12)8-1-4-10(15)5-2-8/h1-7H
887-90-1Relevant academic research and scientific papers
Metal-Free, Visible-Light-Enabled Direct C3-H Arylation of Anthranils
Adak, Tapas,Hashmi, A. Stephen K.,Hu, Chao,Li, Jun,Rudolph, Matthias
, (2020/07/24)
An eosin Y disodium salt-catalyzed photoredox C-H arylation of anthranils is reported. A variety of aryl diazonium tetrafluoroborates were used as aryl sources, providing the C3 cross-coupled products. The in situ generated reactive radicals were trapped by anthranils, providing an alternative method to transition-metal-catalyzed C-H arylations of anthranils. Gold-catalyzed downstream transformations demonstrate the synthetic potential of these valuable building blocks.
