6255-58-9 Usage
Heterocyclic organic compound
Yes
The compound contains a sulfur atom and a five-membered ring with oxygen and sulfur atoms, making it a heterocyclic organic compound.
Structural properties
Unique
The compound has a unique structure that contributes to its reactivity and potential applications in various chemical processes.
Applications
Pharmaceutical and agrochemical production
Due to its structural properties and reactivity, 1,3,2-Benzodioxathiole 2-oxide is used in the production of pharmaceuticals and agrochemicals.
Biological activities
Antifungal and antibacterial properties
The compound has been studied for its potential biological activities, which include antifungal and antibacterial properties.
Intermediate for synthesis
Potential use
1,3,2-Benzodioxathiole 2-oxide has been investigated as an intermediate for the synthesis of other organic compounds, due to its versatile structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6255-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6255-58:
(6*6)+(5*2)+(4*5)+(3*5)+(2*5)+(1*8)=99
99 % 10 = 9
So 6255-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4O3S/c7-10-8-5-3-1-2-4-6(5)9-10/h1-4H
6255-58-9Relevant articles and documents
High yield synthesis of cyclic phosphites, phosphates, sulphites and sulphates of catechol and glycol mediated by hypervalent silicon centres
Kingston,Sudheendra Rao
, p. 4841 - 4844 (2007/10/03)
Room temperature reactions of both tris(catecholato)silicate, M2[Si(o-C6H4O2)3] {M=Na, Et3NH} and glycolato silicate, K2[Si2(O2C2H4)5] with PCl3, POCl3, SOCl2 and SO2Cl2 proceed exothermally and afford easy isolation of the corresponding cyclic derivatives of catechol/glycol (1-8) in high yield, exemplifying the merit of hypervalent silicon centres in synthesis. (Et3NH)2[Si(o-C6H4O2)3] afford near quantitative conversions.