34256-78-5 Usage
Description
(4-bromophenyl)carbamic acid, with the chemical formula C7H6BrNO2, is a derivative of carbamic acid featuring a phenyl ring substituted with a bromine atom. (4-bromophenyl)carbamic acid is known for its versatile chemical structure and properties, making it a significant player in the realm of organic chemistry and pharmaceutical research.
Uses
Used in Pharmaceutical Synthesis:
(4-bromophenyl)carbamic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry:
As a reagent in chemical reactions, (4-bromophenyl)carbamic acid facilitates the construction of diverse organic molecules. Its presence in these reactions can lead to the formation of complex molecular structures that are essential in various chemical and pharmaceutical applications.
Used in Drug Development:
(4-bromophenyl)carbamic acid's potential applications extend to the development of new drugs and materials. Its chemical versatility positions it as a valuable building block for researchers working on innovative pharmaceuticals and materials with novel properties and functions.
Used in Chemical Research:
(4-bromophenyl)carbamic acid serves as an important compound in the field of chemical research. Its unique structure and properties make it a subject of interest for scientists exploring new reactions, mechanisms, and applications in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 34256-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34256-78:
(7*3)+(6*4)+(5*2)+(4*5)+(3*6)+(2*7)+(1*8)=115
115 % 10 = 5
So 34256-78-5 is a valid CAS Registry Number.
34256-78-5Relevant articles and documents
The silver-mediated annulation of arylcarbamic acids and nitrosoarenes toward phenazines
Chen, Fan,Cheng, Jiang,Qian, Peng-Cheng,Wang, Lu
supporting information, (2021/12/17)
A silver-mediated annulation between arylcarbamic acids and nitrosoarenes was developed, leading to phenazines in moderate to good yields with complexity and diversity. This procedure proceeded with the sequential ortho[sbnd] C[sbnd]H functionalization of arylcarbamic acids, insertion to nitroso group and decarboxylative annulation.
