1228556-86-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-2-(2-bromophenyl)glycine hydrochloride is used as a building block in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Organic Chemistry:
In the field of organic chemistry, (R)-2-(2-bromophenyl)glycine hydrochloride serves as a key intermediate in the synthesis of complex organic molecules, contributing to the advancement of chemical research and development.
Used in Neuroscience and Psychiatry:
(R)-2-(2-bromophenyl)glycine hydrochloride is used as a research compound in neuroscience and psychiatry, where it has been studied for its potential therapeutic applications. Its role in understanding the underlying mechanisms of neurological and psychiatric disorders is of significant interest to researchers.
Used in Drug Development:
(R)-2-(2-bromophenyl)glycine hydrochloride is employed in the development of new drugs for the treatment of various medical conditions. Its potential applications in this area highlight its importance in the pharmaceutical and medical industries, as it may contribute to the creation of novel treatments for a wide range of diseases and disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 1228556-86-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1228556-86:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*5)+(3*6)+(2*8)+(1*6)=172
172 % 10 = 2
So 1228556-86-2 is a valid CAS Registry Number.
1228556-86-2Relevant academic research and scientific papers
Stereochemical aspects and the synthetic scope of the SHi at the sulfur atom. Preparation of enantiopure 3-substituted 2,3-dihydro-1,2- benzoisothiazole 1-oxides and 1,1-dioxides
Fernández-Salas, José A.,Rodríguez-Fernández, M. Mercedes,Maestro, M. Carmen,García-Ruano, José L.
supporting information, p. 6046 - 6048 (2014/05/20)
Intramolecular homolytic substitution (SHi) on the sulfur atom at acyclic N-(o-bromobenzyl)sulfinamides takes place with a complete inversion of the configuration and provides an excellent tool to connect N-tert-butanesulfinylimines with enantiopure 3-substituted benzo-fused sulfinamides (1,2-benzoisothiazoline 1-oxides) and the related pharmacologically relevant sulfonamides. the Partner Organisations 2014.
