5680-80-8 | L-Serine methyl ester, HCl

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$15.00	$10.00
5g	97%	in stock	$16.00	$11.00
25g	97%	in stock	$20.00	$14.00
100g	97%	in stock	$63.00	$44.00
500g	97%	in stock	$106.00	$74.00

Description

• Catalog Number: AB46393
• Chemical Name: L-Serine methyl ester, HCl
• CAS Number: 5680-80-8
• Molecular Formula: C4H10ClNO3
• Molecular Weight: 155.5801
• MDL Number: MFCD00063680
• SMILES: COC(=O)C(CO)N.Cl

Computed Properties

• Complexity: 83.4
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3

Upstream Synthesis Route

L-Serine Methyl Ester Hydrochloride is a valuable compound commonly utilized in chemical synthesis processes. With its unique structure and properties, this versatile compound serves as a crucial building block in the creation of various organic molecules and pharmaceutical compounds. Its application in chemical synthesis extends to the formation of peptide bonds, amino acid derivatives, and other complex organic structures. Additionally, L-Serine Methyl Ester Hydrochloride plays a key role in the development of new drug candidates, agricultural chemicals, and other innovative materials through its involvement in various synthetic pathways. Its compatibility with a wide range of reaction conditions and chemistries makes it an indispensable tool for chemists and researchers seeking to design and synthesize novel compounds with precision and efficiency.

Literature

• Acylated serine derivatives: a unique class of arthropod pheromones of the Australian redback spider, Latrodectus hasselti.

  Angewandte Chemie (International ed. in English) 20100308

• Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

  Nature chemical biology 20090101

• Theoretical evidence for pyramidalized bicyclic serine enolates in highly diastereoselective alkylations.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

• Aziridinium from N,N-dibenzyl serine methyl ester: synthesis of enantiomerically pure beta-amino and alpha,beta-diamino esters.

  Organic letters 20060511

• Selective inhibition of divergent seryl-tRNA synthetases by serine analogues.

  FEBS letters 20050815

• The novel and efficient direct synthesis of N,O-acetal compounds using a hypervalent iodine(III) reagent: an improved synthetic method for a key intermediate of discorhabdins.

  Chemical communications (Cambridge, England) 20050407

• Contribution of the anomeric effect to the solution and crystal structure of [1S,2S,6S,7s]-1,6-diaza-4,9-dioxa-2,7-dimethoxycarbonylbicyclo[4.4.1]undecane, a condensation product of L-serine methyl ester with formaldehyde.

  Carbohydrate research 20010115