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L-Serine, N-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, 4-methylbenzenesulfonate (ester) is a complex organic compound that features L-serine, a non-essential amino acid vital for protein synthesis and nucleic acid metabolism. It also includes a phenylmethyl ester, which serves as a protecting group in organic synthesis, and a 4-methylbenzenesulfonate ester group that enhances the stability of the compound. This multifunctional compound has potential applications in pharmaceuticals, organic synthesis, and biochemical research.

16938-05-9

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16938-05-9 Usage

Uses

Used in Pharmaceutical Industry:
L-Serine, N-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, 4-methylbenzenesulfonate (ester) is used as an intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and functional groups. Its presence in protein synthesis and nucleic acid metabolism pathways makes it a valuable component in the development of drugs targeting these biological processes.
Used in Organic Synthesis:
In the field of organic synthesis, L-Serine, N-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, 4-methylbenzenesulfonate (ester) is used as a versatile building block for the creation of more complex organic molecules. The phenylmethyl ester and 4-methylbenzenesulfonate ester groups provide opportunities for further chemical reactions and modifications, making it a useful precursor in the synthesis of a wide range of organic compounds.
Used in Biochemical Research:
L-Serine, N-[(phenylmethoxy)carbonyl]-, phenylmethyl ester, 4-methylbenzenesulfonate (ester) is also utilized in biochemical research as a tool to study the mechanisms of protein synthesis and nucleic acid metabolism. Its unique structure allows researchers to investigate the interactions between amino acids, enzymes, and other biomolecules, contributing to a deeper understanding of these essential biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 16938-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16938-05:
(7*1)+(6*6)+(5*9)+(4*3)+(3*8)+(2*0)+(1*5)=129
129 % 10 = 9
So 16938-05-9 is a valid CAS Registry Number.

16938-05-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-(benzyloxycarbonyl)-O-(p-toluenesulfonyl)serine benzyl ester

1.2 Other means of identification

Product number -
Other names (S)-2-Benzyloxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid benzyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16938-05-9 SDS

16938-05-9Relevant academic research and scientific papers

Utility of tetrathiomolybdate and tetraselenotungstate: Efficient synthesis of cystine, selenocystine, and their higher homologues

Bhat, Ramakrishna G.,Porhiel, Emmanuel,Saravanan, Vadivelu,Chandrasekaran, Srinivasan

, p. 5251 - 5253 (2007/10/03)

Efficient synthesis of cystine, selenocystine, and their higher homologues like homo and bishomo amino acid derivatives from natural amino acid derivatives using tetrathiomolybdate and tetraselenotungstate reagents under mild and neutral conditions is reported. The generality of the reaction has been studied by capping various groups to amino and carboxyl components of canonical amino acids.

Alkylphospho-L-serine analogues: Synthesis of cytostatically active alkylphosphono derivatives

Brachwitz,Oelke,Bergmann,Langen

, p. 1739 - 1742 (2007/10/03)

Hexadecylphosphono-L-seline (2) was synthesised by phospholipase-D- catalysed transesterification of hexadecylphosphonocholine in the presence of L-serine. The synthesis of β-O-hexadecylphosphono-L-alanine (10) starting from N-benzyloxycarbonyl-L-serine benzyl ester is reported. The compounds 2 and 10 were found to cxhibit cytostatic activity in vitro.

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