25216-72-2 Usage
Description
[2-(3-Bromo-phenyl)-ethyl]-carbamic acid methyl ester is a chemical compound with the molecular formula C10H12BrNO2. It is a methyl ester derived from the reaction of carboxylic acid and methanol, featuring a phenyl and bromo group in its structure. [2-(3-BroMo-phenyl)-ethyl]-carbaMic acid Methyl ester is commonly utilized in the synthesis of pharmaceutical compounds and other organic molecules, making it a valuable asset in medicinal chemistry for the development of drugs targeting specific receptors within the body.
Uses
Used in Pharmaceutical Synthesis:
[2-(3-Bromo-phenyl)-ethyl]-carbamic acid methyl ester is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure, which includes a phenyl and bromo group, allows for the creation of molecules with specific receptor-targeting properties, potentially leading to the development of more effective drugs.
Used in Organic Chemistry:
In the field of organic chemistry, [2-(3-Bromo-phenyl)-ethyl]-carbamic acid methyl ester serves as a key building block for the synthesis of a wide range of organic molecules. Its versatility in reactions and the presence of functional groups make it a valuable component in the creation of complex organic structures.
Used in Medicinal Chemistry Research:
[2-(3-BroMo-phenyl)-ethyl]-carbaMic acid Methyl ester is also used as a research tool in medicinal chemistry, where it can help scientists understand the interactions between molecules and biological targets. Further research and testing may be necessary to fully comprehend its potential applications and optimize its use in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 25216-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,1 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25216-72:
(7*2)+(6*5)+(5*2)+(4*1)+(3*6)+(2*7)+(1*2)=92
92 % 10 = 2
So 25216-72-2 is a valid CAS Registry Number.
25216-72-2Relevant articles and documents
Copper-Catalyzed Coupling of Amines with Carbazates: An Approach to Carbamates
Wang, Song-Ning,Zhang, Guo-Yu,Shoberu, Adedamola,Zou, Jian-Ping
, p. 9067 - 9075 (2021/07/19)
A new approach for the preparation of carbamatesviathe copper-catalyzed cross-coupling reaction of amines with alkoxycarbonyl radicals generated from carbazates is described. This environmentally friendly protocol takes place under mild conditions and is compatible with a wide range of amines, including aromatic/aliphatic and primary/secondary substrates.
Factor XIa Inhibitors
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Paragraph 0304; 0305, (2016/09/12)
The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses, embolisms, hypercoagulability or fibrotic changes.
Hindered ureas as masked isocyanates: Facile carbamoylation of nucleophiles under neutral conditions
Hutchby, Marc,Houlden, Chris E.,Gair Ford,Tyler, Simon N. G.,Gagne, Michel R.,Lloyd-Jones, Guy C.,Booker-Milburn, Kevin I.
supporting information; experimental part, p. 8721 - 8724 (2010/01/16)
Bigger is better: Sterically hindered dialkyl ureas undergo nucleophilic substitution at dramatically faster rates than their less hindered counterparts (see scheme). Steric decompression upon the formation of an intermediate isocyanate can explain this c
