19525-87-2 Usage
Description
O-Benzyl-L-serine Methyl Ester Hydrochloride is an organic compound that serves as a key reactant in the synthesis of various pharmaceutical and chemical compounds. It is characterized by its unique structure, which includes a benzyl group attached to the L-serine molecule and a methyl ester functional group. O-BENZYL-L-SERINE METHYL ESTER HYDROCHLORIDE is highly valuable in the field of organic synthesis due to its reactivity and versatility.
Uses
Used in Pharmaceutical Industry:
O-Benzyl-L-serine Methyl Ester Hydrochloride is used as a reactant for the synthesis of ureidopeptides and peptidyl ureas. These compounds are important in the development of novel drugs with potential therapeutic applications. The use of this reactant allows for the creation of diverse and complex molecular structures, which can be tailored to target specific biological pathways or receptors.
In the synthesis of ureidopeptides and peptidyl ureas, O-Benzyl-L-serine Methyl Ester Hydrochloride plays a crucial role in forming the backbone of these molecules. The benzyl group provides steric hindrance and electronic effects that can influence the reactivity and selectivity of the reaction, while the methyl ester group can be used for further functionalization or as a protecting group during the synthesis process.
The applications of ureidopeptides and peptidyl ureas are vast, ranging from the development of new antibiotics to the design of potent enzyme inhibitors. These compounds can also be used as building blocks for the construction of larger peptide-based drugs or as components of drug delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 19525-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,2 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19525-87:
(7*1)+(6*9)+(5*5)+(4*2)+(3*5)+(2*8)+(1*7)=132
132 % 10 = 2
So 19525-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c1-14-11(13)10(12)8-15-7-9-5-3-2-4-6-9/h2-6,10H,7-8,12H2,1H3
19525-87-2Relevant articles and documents
Gram-Scale Solution-Phase Synthesis of Heptapeptide Side Chain of Teixobactin 1
Chandrasekhar, Srivari,Donikela, Sangeetha,Mainkar, Prathama S.,Nayani, Kiranmai,Nomula, Vishnuvardhan
supporting information, p. 2268 - 2272 (2019/12/11)
We report herein a scalable synthesis of linear heptapeptide side chain of the depsipeptide natural product teixobactin through solution phase. The synthesis of heptapeptide was achieved through an efficient coupling of suitably protected tripeptide and tetrapeptide comprising of three d-amino acids and four usual l-amino acid subunits.
Continuous multiple liquid-liquid separation: Diazotization of amino acids in flow
Hu, Dennis X.,O'Brien, Matthew,Ley, Steven V.
supporting information; experimental part, p. 4246 - 4249 (2012/10/08)
A second-generation laboratory-scale, modular liquid-liquid separation device based on computer-controlled high-pressure pumps and a high-resolution digital camera has been invented. The diazotization of amino acids to produce valuable chiral hydroxyacids is demonstrated in flow for the first time. The use of a triple-separator system in conjuction with the developed diazotization process allows the safe and efficient production and automated isolation of multigram quantities of valuable chiral hydroxyacids.
New efficient enantioselective synthesis of 2-oxopiperazines: a practical access to chiral 3-substituted 2-oxopiperazines
Lencina, Claiton Leoneti,Dassonville-Klimpt, Alexandra,Sonnet, Pascal
, p. 1689 - 1697 (2008/12/21)
The development of efficient and stereoselective methods to produce 1,4-disubstituted-2-oxopiperazine in enantiomerically pure form, from a readily available starting material is crucial. Herein, we report a reduction modification to our previously descri
