800400-79-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-Bromo-5,6-dichloro-1H-indol-3-yl)ethanone is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure, including the halogen atoms and the indole ring, makes it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
1-(2-Bromo-5,6-dichloro-1H-indol-3-yl)ethanone is used as a key building block in the synthesis of complex organic molecules. The presence of the bromine and chlorine atoms allows for further functionalization and modification of the molecule, enabling the creation of a wide range of chemical products with diverse applications.
Used in Research and Development:
1-(2-Bromo-5,6-dichloro-1H-indol-3-yl)ethanone is utilized as a research compound for studying the properties and potential applications of indole-based compounds. Its unique structure and the presence of halogen atoms make it an interesting subject for scientific investigation, which could lead to the discovery of new synthetic methods, pharmaceuticals, or other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 800400-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,0,4,0 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 800400-79:
(8*8)+(7*0)+(6*0)+(5*4)+(4*0)+(3*0)+(2*7)+(1*9)=107
107 % 10 = 7
So 800400-79-7 is a valid CAS Registry Number.
800400-79-7Relevant academic research and scientific papers
Synthesis, antiviral activity, and mode of action of some 3-substituted 2,5,6-trichloroindole 2′- and 5″-deoxyribonucleosides
Williams, John D.,Ptak, Roger G.,Drach, John C.,Townsend, Leroy B.
, p. 5773 - 5782 (2007/10/03)
A series of chlorinated indole nucleosides has been synthesized and tested for activity against human cytomegalovirus (HCMV) and herpes simplex virus type-1 (HSV-1) and for cytotoxicity. The 2′- and 5′-deoxy derivatives of the reported 3-formyl-2,5,6-tric
