96129-73-6 Usage
Uses
Used in Pharmaceutical Industry:
4,7-Dichloroindole is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its potential antitumor and antimicrobial properties make it a valuable component in the development of new drugs and treatments.
Used in Organic Semiconductors Development:
4,7-Dichloroindole is used as a key component in the development of organic semiconductors. Its unique properties contribute to the advancement of organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells.
Used in Antitumor Research:
4,7-Dichloroindole is used as a subject of study for its potential antitumor properties. Researchers are exploring its ability to inhibit tumor growth and progression, offering new avenues for cancer treatment and therapy.
Used in Antimicrobial Applications:
4,7-Dichloroindole is used as an antimicrobial agent, demonstrating potential in combating various types of bacteria and other microorganisms. Its effectiveness in this area could lead to the development of new antimicrobial products and treatments.
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 academic research and scientific papers
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.
