156042-32-9 Usage
Description
L-Serine, N-(1-oxohexadecyl)-, tetradecyl ester is a compound that consists of a serine molecule attached to a long-chain fatty acid known as tetradecyl ester. This chemical is a derivative of the amino acid L-Serine, which plays a key role in the synthesis of proteins and other important molecules in the body. The attachment of the fatty acid ester to the serine molecule allows it to interact with cell membranes and lipids, potentially influencing cellular processes and functions.
Uses
Used in Biochemistry:
L-Serine, N-(1-oxohexadecyl)-, tetradecyl ester is used as a research tool for studying the interactions between amino acids and lipids in cellular membranes and their effects on cellular processes.
Used in Pharmaceuticals:
L-Serine, N-(1-oxohexadecyl)-, tetradecyl ester is used as a potential therapeutic agent for targeting specific cellular processes and functions, given its ability to interact with cell membranes and lipids.
Used in Cosmetics:
L-Serine, N-(1-oxohexadecyl)-, tetradecyl ester is used as an ingredient in cosmetic formulations for its potential moisturizing and skin conditioning properties, as it can interact with lipids in the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 156042-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,0,4 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 156042-32:
(8*1)+(7*5)+(6*6)+(5*0)+(4*4)+(3*2)+(2*3)+(1*2)=109
109 % 10 = 9
So 156042-32-9 is a valid CAS Registry Number.
156042-32-9Relevant articles and documents
PMS synthesis method
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, (2021/02/10)
The invention discloses a PMS synthesis method, and belongs to the technical field of organic synthesis. The method comprises the following steps: reacting L-serine methyl ester hydrochloride with palmitoyl chloride to obtain N-palmitoyl-L-serine methyl ester; carrying out benzyl protection on the N-palmitoyl-L-serine methyl ester, and hydrolyzing the methyl ester to obtain N-palmitoyl-O-benzyl-L-serine; esterifying the N-palmitoyl-O-benzyl-L-serine and tetradecyl alcohol to obtain N-palmitoyl-O-benzyl-L-serine tetradecyl ester; and finally, debenzylating the N-palmitoyl-O-benzyl-L-serine tetradecyl ester to obtain the PMS. According to the invention, cheap L-serine methyl ester hydrochloride is used as a raw material, and benzyl is used for protecting hydroxyl, so that the side reaction of esterification with tetradecyl alcohol when the hydroxyl in a serine parent is not protected is effectively avoided, the reaction conversion rate is improved, the difficulty of separation and purification caused by byproducts is reduced, and the method can be effectively suitable for industrial mass production.