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96854-24-9

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96854-24-9 Usage

Description

N-(Methoxycarbonyl)-L-serine Methyl Ester is an organic compound that serves as an important intermediate in the synthesis of various biologically active molecules. It is characterized by the presence of a methoxycarbonyl group and a methyl ester group attached to the L-serine backbone, which contributes to its unique chemical properties and reactivity.

Uses

Used in Biochemical Research:
N-(Methoxycarbonyl)-L-serine Methyl Ester is used as a key building block for the synthesis of complex carbohydrates and glycoconjugates, which are essential for understanding the structure and function of various biological systems.
Used in Pharmaceutical Industry:
N-(Methoxycarbonyl)-L-serine Methyl Ester is used as a synthetic precursor for the production of therapeutic agents, particularly those targeting carbohydrate-related diseases and disorders.
Used in the Synthesis of Tn Antigen:
N-(Methoxycarbonyl)-L-serine Methyl Ester is used as a crucial component in the synthesis of Tn antigen (GalNAc-α-O-Ser), which possesses significant biological properties and is involved in various cellular processes, including cell adhesion, immune response, and cell signaling.

Check Digit Verification of cas no

The CAS Registry Mumber 96854-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96854-24:
(7*9)+(6*6)+(5*8)+(4*5)+(3*4)+(2*2)+(1*4)=179
179 % 10 = 9
So 96854-24-9 is a valid CAS Registry Number.

96854-24-9Relevant articles and documents

Process for a phenylthiobutyl-isoquinoline and intermediates therefor

-

, (2008/06/13)

The present invention relates to a new method for making compounds of formula and intermediates for making compounds of formual II. The compounds of this invention are useful intermediates for the manufacture of pharmacologically active compounds suitable

Enantiospecific synthesis of R- and S-5,6-dihydroxy-2-(N,N-di-n-propylamino)tetralins from serine

Baxter,Murray,Taylor

, p. 2331 - 2334 (2007/10/02)

The first enantiospecific synthesis of 5,6-dihydroxy-2-(N,N-di-n-propylamino)tetralin [5,6-(HO)2DPAT] is reported. Starting from D- or L-serine either enantiomer is readily available in high optical purity.

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