130406-35-8 Usage
Description
(R)-(2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester is a compound utilized in the field of medicinal chemistry, characterized by its benzyl ester derivative nature of carbamic acid and the presence of an amino group and a phenyl group. This chemical is distinguished by its stereochemistry, which provides a specific three-dimensional arrangement of its atoms, potentially influencing its pharmacological properties. Further research and experimentation are essential to explore its full potential in the development of pharmaceuticals, where it could serve as a precursor or intermediate in the synthesis of biologically active compounds.
Uses
Used in Pharmaceutical Development:
(R)-(2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester is used as a precursor or intermediate in the pharmaceutical industry for the synthesis of biologically active compounds. Its unique structure and stereochemistry make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-(2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester is used as a research compound to study its potential interactions with biological targets and its effects on various physiological processes. This may lead to the discovery of new therapeutic approaches and the creation of novel pharmaceuticals.
Used in Drug Synthesis:
(R)-(2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester is employed as a key component in the synthesis of various drugs, particularly those targeting specific receptors or enzymes in the body. Its unique structural features and stereochemistry may contribute to the development of more effective and selective medications.
Used in Stereochemistry Studies:
In the field of stereochemistry, (R)-(2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester serves as a model compound to investigate the impact of stereochemistry on the pharmacological properties of molecules. This research can provide valuable insights into the design of more effective drugs with improved selectivity and reduced side effects.
Used in Drug Design and Optimization:
(R)-(2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester is utilized in the process of drug design and optimization, where its unique structural features and stereochemistry can be leveraged to create more potent and selective drug candidates. This may lead to the development of new therapeutic agents with better efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 130406-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,0 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130406-35:
(8*1)+(7*3)+(6*0)+(5*4)+(4*0)+(3*6)+(2*3)+(1*5)=78
78 % 10 = 8
So 130406-35-8 is a valid CAS Registry Number.
130406-35-8Relevant articles and documents
Rationally Designed "Dipeptoid" Analogues of CCK. α-Methyltryptophan Derivatives as Highly Selective and Orally Active Gastrin and CCK-B Antagonists with Potent Anxiolytic Properties
Horwell, David C.,Hughes, John,Hunter, John C.,Pritchard, Martyn C.,Richardson, Reginald S.,at al.
, p. 404 - 414 (2007/10/02)
This paper describes the synthesis and structure-activity relationships (SAR) leading to the first rational design of "dipeptoid" analogues of the neuropeptide cholecystokinin (CCK).Compounds *,S*)>-4-2-3-(1H-indol-3-yl)-2-m
