192328-48-6 Usage
Uses
Used in Pharmaceutical Research and Development:
(R)-Amino-(3-bromo-4-methoxy-phenyl)-acetic acid methyl ester is used as an intermediate in the synthesis of various pharmaceutical drugs. Its unique structure and chirality allow for the development of novel compounds with potential therapeutic applications.
Used in Drug Synthesis:
In the pharmaceutical industry, (R)-Amino-(3-bromo-4-methoxy-phenyl)-acetic acid methyl ester is used as a key building block for creating new drug candidates. Its bromo and methoxy substituents on the phenyl ring provide opportunities for further chemical modifications, leading to the development of innovative medications with improved efficacy and selectivity.
Used in Chiral Chemistry:
(R)-Amino-(3-bromo-4-methoxy-phenyl)-acetic acid methyl ester is used as a chiral molecule in the study of stereochemistry and asymmetric synthesis. Understanding the properties and reactivity of its enantiomeric forms can contribute to the advancement of chiral drug design and the development of enantioselective synthetic methods.
Used in Biological Studies:
(R)-Amino-(3-bromo-4-methoxy-phenyl)-acetic acid methyl ester may have biological activity in its own right, making it a candidate for further investigation into its potential therapeutic effects. Research in this area could lead to the discovery of new pharmacological applications for (R)-Amino-(3-bromo-4-methoxy-phenyl)-acetic acid methyl ester.
Check Digit Verification of cas no
The CAS Registry Mumber 192328-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,3,2 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 192328-48:
(8*1)+(7*9)+(6*2)+(5*3)+(4*2)+(3*8)+(2*4)+(1*8)=146
146 % 10 = 6
So 192328-48-6 is a valid CAS Registry Number.
192328-48-6Relevant academic research and scientific papers
Synthesis of the vancomycin CD and DE ring systems
Boger, Dale L.,Borzilleri, Robert M.,Nukui, Seiji,Beresis, Richard T.
, p. 4721 - 4736 (2007/10/03)
Full details of the synthesis of the fully substituted vancomycin CD and DE ring systems are described and a potential solution to the control of the atropisomer stereochemistry is defined.
