164334-69-4 Usage
Description
3-Bromo-4'-chlorobiphenyl, also known as 3-Bromo-4'-chloro-1,1'-biphenyl, is a type of hydrocarbon organic compound characterized by the presence of a bromine atom at the 3rd position and a chlorine atom at the 4' position on the biphenyl molecule. 3-Bromo-4'-chlorobiphenyl is known for its unique chemical properties and structural features, which make it a versatile molecule for various applications.
Uses
Used in Pharmaceutical Industry:
3-Bromo-4'-chlorobiphenyl is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to serve as a building block or a key component in the development of new pharmaceutical compounds, contributing to the advancement of medical treatments and therapies.
As a pharmaceutical intermediate, 3-Bromo-4'-chlorobiphenyl plays a crucial role in the development of drugs targeting a wide range of health conditions and diseases. Its chemical properties enable it to be modified and functionalized to create new molecules with specific therapeutic effects, making it a valuable asset in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 164334-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,3,3 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 164334-69:
(8*1)+(7*6)+(6*4)+(5*3)+(4*3)+(3*4)+(2*6)+(1*9)=134
134 % 10 = 4
So 164334-69-4 is a valid CAS Registry Number.
164334-69-4Relevant articles and documents
Visible-Light-Promoted, Catalyst-Free Gomberg-Bachmann Reaction: Synthesis of Biaryls
Lee, Juyoung,Hong, Boseok,Lee, Anna
, p. 9297 - 9306 (2019/08/12)
Biaryls were synthesized via a novel visible-light-promoted Gomberg-Bachmann reaction that does not require a photosensitizer or any metal reagents. The formation of an electron donor-acceptor complex between aryl diazonium salts and pyridine allows, under visible-light irradiation, the synthesis of biaryls in moderate-to-high yields.
