65685-55-4 Usage
General Description
1,2-Benzisoxazol-6-ol, also known as benzisoxazolol or 6-hydroxybenzisoxazole, is a chemical compound with the molecular formula C7H5NO2. It is a heterocyclic compound that contains both benzene and isoxazole rings. 1,2-Benzisoxazol-6-ol is used in the production of various pharmaceuticals, particularly in the synthesis of drugs with psychotropic and neuroleptic properties. It also has potential applications in the field of organic electronics as a versatile building block for the synthesis of functional organic materials. Additionally, 1,2-Benzisoxazol-6-ol has been studied for its antimicrobial and antidiabetic properties, showing potential for use in the development of new therapeutic agents. However, it is important to handle and use this compound with caution, as it may have harmful effects on human health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 65685-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,8 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65685-55:
(7*6)+(6*5)+(5*6)+(4*8)+(3*5)+(2*5)+(1*5)=164
164 % 10 = 4
So 65685-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NO2/c9-6-2-1-5-4-8-10-7(5)3-6/h1-4,9H
65685-55-4Relevant articles and documents
Triflic anhydride: A mild reagent for highly efficient synthesis of 1,2-benzisoxazoles, isoxazolo, and isothiazolo quinolines without additive or base
Kalkhambkar, Rajesh G.,Yuvaraj
supporting information, p. 547 - 555 (2014/01/23)
The synthetic utility of trifluoromethanesulphonic anhydride (triflic anhydride, TA) without additive or base for the high-yielding synthesis of a wide variety of 1,2-benzisoxazoles from 2-hydroxyaryl aldoximes and ketoximes under mild conditions has been carried out for the first time. As a continuation of our study, syntheses of isoxazolo and isothiazolo quinolones have also been demonstrated using triflic anhydride under similar conditions. This method is simple and has benefits from the easy way to isolate the products in excellent yields.
