181140-88-5 Usage
Description
(R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID, a chemical compound with the molecular formula C17H25NO4, is a derivative of the amino acid phenylalanine. It is commonly used in organic synthesis and pharmaceutical research due to its tert-butoxycarbonyl (Boc) protecting group, which ensures the stability of the amino group during chemical reactions. (R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID serves as a building block for the synthesis of peptide-based drugs and has potential applications in the development of new pharmaceuticals and bioactive molecules. Furthermore, it has been studied for its potential anti-inflammatory and analgesic properties.
Uses
Used in Pharmaceutical Research and Development:
(R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is used as a building block for the synthesis of peptide-based drugs, contributing to the development of new pharmaceuticals and bioactive molecules. Its Boc protecting group allows for stable and efficient chemical reactions in the synthesis process.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is utilized for the preparation of various organic compounds, taking advantage of its unique structure and reactivity.
Used in Anti-inflammatory and Analgesic Applications:
(R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is studied for its potential anti-inflammatory and analgesic properties, indicating its possible use in the development of medications for pain relief and inflammation management.
Used in the Pharmaceutical Industry:
(R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds, playing a crucial role in the development of novel drugs and therapies.
Used in the Bioactive Molecule Development:
(R)-3-(TERT-BUTOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is employed in the development of bioactive molecules, which have potential applications in various therapeutic areas, including but not limited to, oncology, neurology, and immunology.
Check Digit Verification of cas no
The CAS Registry Mumber 181140-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,1,4 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 181140-88:
(8*1)+(7*8)+(6*1)+(5*1)+(4*4)+(3*0)+(2*8)+(1*8)=115
115 % 10 = 5
So 181140-88-5 is a valid CAS Registry Number.
181140-88-5Relevant articles and documents
Copper-catalyzed borylative aminomethylation of C-C double and triple bonds withN,O-acetal
Qiu, Xianfan,Xu, Liugen,Wang, Shuxia,Dai, Ying,Feng, Yunqiu,Gong, Chang,Tao, Chuanzhou
, p. 3279 - 3282 (2021/04/07)
A copper-catalyzed borylaminomethylation of multiple carbon-carbon bonds withN,O-acetal and bis(pinacolato)diboron has been disclosed that offers efficient and expedient access to γ-amino boronates. The products contain a valuable amine and boronate, whic
Nucleoside derivatives for library preparation
-
, (2008/06/13)
Nucleoside derivatives as building blocks for templated libraries are described.
Palladium-catalysed asymmetric allylic substitution: Synthesis of α- and β-amino acids
Bower, Justin F.,Jumnah, Roshan,Williams, Andrew C.,Williams, Jonathan M. J.
, p. 1411 - 1420 (2007/10/03)
Methodology has been established for the formation of enantiomerically enriched α-amino acids using palladium-catalysed allylic amination. The formation of enantiomerically enriched allylamines has been achieved with high enantioselectivity. Oxidative cleavage of the allylamines provides arylglycine and glutamic acid derivatives. Additionally, enantiomerically enriched β-amino acids have been prepared in high enantiomeric excess. Palladium-catalysed asymmetric allylic substitution is used as the key synthetic transformation.
