96129-73-6 Usage
General Description
4,7-Dichloroindole is a chemical compound with the molecular formula C8H5Cl2N. It is a derivative of indole, a heterocyclic aromatic organic compound. 4,7-Dichloroindole is commonly used as a building block for the synthesis of various pharmaceuticals and agrochemicals. It has been studied for its potential antitumor and antimicrobial properties. Additionally, it has shown to have potential application in the development of organic semiconductors. The compound is recognized for its wide range of applications in the fields of medicine and materials science, making it an important subject of study for researchers in various scientific disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 96129-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96129-73:
(7*9)+(6*6)+(5*1)+(4*2)+(3*9)+(2*7)+(1*3)=156
156 % 10 = 6
So 96129-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2N/c9-6-1-2-7(10)8-5(6)3-4-11-8/h1-4,11H
96129-73-6Relevant articles and documents
Solution and Flash Vacuum Pyrolysis of Some 2,6-Disubstituted β-Phenethylsulfonyl Azides and of β-Styrenesulfonyl Azide
Abramovitch, Rudolph A.,Kress, Albert O.,Pillay, Kutten S.,Thompson, W. Marshall
, p. 2066 - 2073 (2007/10/02)
Solution thermolysis of 2,6-dichloro-β-phenethyl- and 2,6-dimethyl-β-phenethylsulfonyl azide leads to the formation of the corresponding 5,8-disubstituted 3,4-dihydro-2,1-benzothiazine 2,2-dioxides resulting from a 1,2-chlorine and -methyl shift, respectively, in the intermediates.No insertion into the phenethyl side chain, or into the side-chain methyl group in the 2,6-dimethyl case, was detected.Attempted cyclization of ethene-sulfonanilides to 2,1-benzothiazine 2,2-dioxide failed.The orientation of the dichlorosultam was established unambiguously by its FVP to 4,7-dichloroindoline and by the synthesis of an authentic sample.Solution thermolysis of β-styrenesulfonyl azide gave only hydrogen abstraction (32) and solvent insertion (33) products, but FVP gave indole, phenylacetonitrile, and phenylacetylene.
