1060802-88-1 Usage
Description
6-Bromo-1,2-benzisoxazole is an organic compound characterized by the presence of a bromine atom at the 6th position and a benzene ring fused to an isoxazole ring. It is a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds.
Uses
Used in Organic Synthesis:
6-Bromo-1,2-benzisoxazole is used as a research reagent for organic synthesis, particularly in the development of new chemical compounds and processes. Its unique structure and reactivity make it a versatile building block for creating a wide range of organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-bromo-1,2-benzisoxazole is used as a key intermediate in the synthesis of various drug candidates. Its presence in the molecular structure can impart specific biological activities, making it an essential component in the development of new medications.
Used in Agrochemical Industry:
6-Bromo-1,2-benzisoxazole is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness in controlling pests and diseases, contributing to increased crop yields and food security.
Overall, 6-bromo-1,2-benzisoxazole is a significant compound in the fields of organic synthesis, pharmaceuticals, and agrochemicals, playing a crucial role in the development of new and improved products.
Check Digit Verification of cas no
The CAS Registry Mumber 1060802-88-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,8,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1060802-88:
(9*1)+(8*0)+(7*6)+(6*0)+(5*8)+(4*0)+(3*2)+(2*8)+(1*8)=121
121 % 10 = 1
So 1060802-88-1 is a valid CAS Registry Number.
1060802-88-1Relevant articles and documents
An efficient synthesis of oxazolines: Via a cascade reaction between azaoxyallyl cations and 1,2-benzisoxazoles
Sun, Li,Liu, Yi,Wang, Yankai,Li, Yuanyuan,Liu, Zhiwen,Lu, Tao,Li, Wenhai
supporting information, p. 7526 - 7530 (2019/08/20)
A formal [3 + 2] cycloaddition reaction between the C and O terminals of azaoxyallyl cations formed in situ and 1,2-benzisoxazoles has been realized. This one-pot cycloaddition method provided an effective and practical pathway to synthesize oxazoline in good yields under mild conditions. The title products exhibited unique fluorescence properties.
