877078-00-7 Usage
General Description
6-Quinoxalinesulfonyl chloride, 2-chloro- is a chemical compound with the molecular formula C8H5ClN2O2S. It is a sulfonyl chloride derivative of quinoxaline, with a chlorine atom substituted at the 2-position of the quinoxaline ring. 6-Quinoxalinesulfonyl chloride, 2-chloro- is commonly used in organic synthesis as a reagent for the preparation of various quinoxaline derivatives. It is known for its ability to react with a variety of nucleophiles, including amines and heterocyclic compounds, to form a wide range of functionalized quinoxaline derivatives. Additionally, 6-Quinoxalinesulfonyl chloride, 2-chloro- has been studied for its potential applications in the development of pharmaceuticals and agrochemicals. Due to its versatile reactivity and potential medical and agricultural applications, this compound is of interest to researchers in the fields of organic synthesis and chemical biology.
Check Digit Verification of cas no
The CAS Registry Mumber 877078-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,0,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 877078-00:
(8*8)+(7*7)+(6*7)+(5*0)+(4*7)+(3*8)+(2*0)+(1*0)=207
207 % 10 = 7
So 877078-00-7 is a valid CAS Registry Number.
InChI:InChI=1S/C8H4Cl2N2O2S/c9-8-4-11-7-3-5(15(10,13)14)1-2-6(7)12-8/h1-4H
877078-00-7Relevant articles and documents
Synthesis and antimicrobial activity of some 2(1H)-quinoxalinone-6-sulfonyl derivatives
Obafemi, Craig A.,Akinpelu
, p. 1795 - 1807 (2007/10/03)
The synthesis of some quinoxalinesulfonyl derivatives is described. Two of the synthesized derivatives, 2-oxo-1,2-dihydroquinoxaline-6-sulfonyl azide (3a) and 2,3-dioxo-1,2,3,4-tetrahydroquinoxaline-6-sulfonyl azide (3b), were screened in vitro for their growth inhibitory activity against nine strains of Gram-positive and seven strains of Gram-negative bacteria, along with two fungal isolates. The two compounds showed broad spectrum (in vitro) activity against the bacterial strains. Copyright Taylor & Francis Inc.
