33757-34-5 Usage
Description
(3-BromoPhenyl)(4-Methylphenyl)Methanol is a chemical compound that features a bromine atom attached to a phenyl ring and a methyl group attached to another phenyl ring, both connected to a central methanol molecule. (3-BroMophenyl)(4-Methylphenyl)Methanol is known for its potential applications in organic synthesis, pharmaceutical research, and as a precursor in the production of various pharmaceutical drugs. It also holds promise for its potential biological activities and its role in the development of new therapeutic agents. However, it is crucial to handle this compound with care due to its potentially hazardous nature.
Uses
Used in Organic Synthesis:
(3-BromoPhenyl)(4-Methylphenyl)Methanol is used as a building block in organic synthesis for creating more complex molecules. Its unique structure allows for various chemical reactions to produce a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3-BromoPhenyl)(4-Methylphenyl)Methanol is used as a reagent in chemical reactions, contributing to the development of new drugs and therapeutic agents.
Used as a Precursor in Drug Production:
(3-BromoPhenyl)(4-Methylphenyl)Methanol serves as a precursor in the production of various pharmaceutical drugs, playing a crucial role in the synthesis of active pharmaceutical ingredients.
Used in Biological Activity Studies:
(3-BroMophenyl)(4-Methylphenyl)Methanol has been studied for its potential biological activities, which may lead to the discovery of new therapeutic agents and treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 33757-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,5 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33757-34:
(7*3)+(6*3)+(5*7)+(4*5)+(3*7)+(2*3)+(1*4)=125
125 % 10 = 5
So 33757-34-5 is a valid CAS Registry Number.
33757-34-5Relevant articles and documents
Orthoplatinated triarylphosphite as a highly efficient catalyst for addition reactions of arylboronic acids with aldehydes: Low catalyst loading catalysis and a new tandem reaction sequence
Liao, Yuan-Xi,Xing, Chun-Hui,He, Ping,Hu, Qiao-Sheng
supporting information; experimental part, p. 2509 - 2512 (2009/05/26)
(Chemical Equation Presented) Readily available, air/moisture-stable orthoplatinated triarylphosphite catalyzes the addition reactions of arylboronic acids with aldehydes with the catalyst loading as low as 0.01%. It also cataylzes a new tandem reaction of arylboronic acids with α,β- unsaturated aldehydes to form 1,3-diaryl-1-propanols. Our study provides a new paradigm for the application of orthoplatinated triarylphosphites, and may pave the road to develop other Pt(II) catalysts for such addition reactions and other tandem reactions with such addition reactions as part of the reaction sequence.
Process for producing benzhydrols
-
, (2008/06/13)
There is disclosed a process for producing benzhydrls by reacting an arylmetal compound with an aromatic aldehyde. According to this process, benzhydrols useful as raw materials for medicines and photopolymerization initiators can be produced in a high yield and industrially advantageously.
