39835-07-9 Usage
Description
6-Chloro-1,2-benzisoxazole is a heterocyclic aromatic organic compound with the molecular formula C7H4ClNO. It features a benzene ring fused to an isoxazole ring, with a chlorine atom at position 6. 6-CHLORO-1,2-BENZISOXAZOLE is known for its versatile chemical reactivity and potential pharmacological properties, making it a valuable building block in the synthesis of various chemicals and materials.
Uses
Used in Pharmaceutical Synthesis:
6-Chloro-1,2-benzisoxazole is used as a key intermediate in the synthesis of pharmaceuticals for its versatile chemical reactivity. It contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 6-chloro-1,2-benzisoxazole is utilized as a building block in the production of various agrochemicals. Its chemical properties allow for the creation of compounds with pesticidal or herbicidal activities, contributing to crop protection and yield enhancement.
Used in Organic Compound Synthesis:
6-Chloro-1,2-benzisoxazole serves as a versatile starting material in the synthesis of a wide range of organic compounds. Its unique structure and reactivity enable the formation of diverse chemical entities for various applications, including materials science and specialty chemicals.
Used in Neuroprotective Agent Development:
6-Chloro-1,2-benzisoxazole has demonstrated potential as a neuroprotective agent. It is being studied for its potential use in the treatment of neurodegenerative diseases, where its pharmacological properties may contribute to the preservation and restoration of neuronal function.
Used in Chemical and Material Production:
As a building block, 6-chloro-1,2-benzisoxazole is employed in the production of various chemicals and materials. Its unique structure and reactivity allow for the creation of compounds with specific properties, such as improved stability, reactivity, or selectivity, which can be applied across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 39835-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39835-07:
(7*3)+(6*9)+(5*8)+(4*3)+(3*5)+(2*0)+(1*7)=149
149 % 10 = 9
So 39835-07-9 is a valid CAS Registry Number.
39835-07-9Relevant 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.