1263377-20-3 Usage
Uses
Used in Organic Synthesis:
1-bromo-3-(tert-butyl)-5-chlorobenzene is used as a reagent in organic synthesis for various chemical reactions and transformation processes. Its high chemical reactivity allows it to participate in a wide range of reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
As an intermediate, 1-bromo-3-(tert-butyl)-5-chlorobenzene plays a crucial role in the production of pharmaceuticals. Its unique structure and reactivity enable the synthesis of various drug molecules, contributing to the development of new medications and therapies.
Used in Agrochemical Production:
1-bromo-3-(tert-butyl)-5-chlorobenzene is also utilized as an intermediate in the production of agrochemicals. Its involvement in the synthesis of agrochemicals helps in the development of effective pesticides, herbicides, and other agricultural products that are essential for maintaining crop health and productivity.
Environmental and Health Considerations:
Due to the potential health hazards and environmental impacts associated with 1-bromo-3-(tert-butyl)-5-chlorobenzene, it is essential to follow proper handling and disposal guidelines. This ensures the safety of workers and minimizes the environmental footprint of its production and use.
Check Digit Verification of cas no
The CAS Registry Mumber 1263377-20-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,3,7 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1263377-20:
(9*1)+(8*2)+(7*6)+(6*3)+(5*3)+(4*7)+(3*7)+(2*2)+(1*0)=153
153 % 10 = 3
So 1263377-20-3 is a valid CAS Registry Number.
1263377-20-3Relevant academic research and scientific papers
Krzeszewski, Maciej,Dobrzycki, ?ukasz,Sobolewski, Andrzej L.,Cyrański, Micha? K.,Gryko, Daniel T.
, p. 14998 - 15005 (2021)
A bowl-shaped nitrogen-doped nanographene composed of a pyrrolo[3,2-b]pyrrole core substituted with six arene rings circularly bonded with one another has been prepared via a concise synthetic strategy encompassing the multicomponent tetraarylpyrrolopyrrole (TAPP) synthesis, the Scholl reaction, and intramolecular direct arylation. This synthesis represents the first case of programmed sequential intramolecular direct arylation reactions utilizing the different reactivity of C–Br and C–Cl bonds. The target compound contains two central pentagons confined between two adjacent heptagons—the inverse Stone–Thrower–Wales topology. The presence of both five- and seven-membered rings in the final structure is responsible for interesting properties such as a perpendicularly aligned dipole moment, absorption and fluorescence in the orange-red region, weak emission originating from the charge-transfer character of a low-energy absorption band, and a high lying HOMO. In the solid state slipped convex-to-convex π–π stacking dominates.
