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223131

DL-Serine methyl ester hydrochloride

Name: <SC>DL</SC>-Serine methyl ester hydrochloride
Brand: ALDRICH

98%

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About This Item

Linear Formula:

HOCH₂CH(NH₂)CO₂CH₃·HCl

CAS Number:

5619-04-5

Molecular Weight:

155.58

NACRES:

NA.22

PubChem Substance ID:

24853368

UNSPSC Code:

12352209

EC Number:

227-047-1

MDL number:

MFCD00012593

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Properties

Quality Level

100

assay

98%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

134-136 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cl[H].COC(=O)C(N)CO

InChI

1S/C4H9NO3.ClH/c1-8-4(7)3(5)2-6;/h3,6H,2,5H2,1H3;1H

InChI key

NDBQJIBNNUJNHA-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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

Carlos Aydillo et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 13(17), 4840-4848 (2007-03-17)

A new chiral serine equivalent and its enantiomer have been synthesized from (S)- and (R)-N-Boc-serine methyl esters (Boc: tert-butyloxycarbonyl). The use of these compounds as chiral building blocks has been demonstrated in the synthesis of alpha-alkyl alpha-amino acids by diastereoselective

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

Dragana Ahel et al.

FEBS letters, 579(20), 4344-4348 (2005-08-02)

Seryl-tRNA synthetases (SerRSs) fall into two distinct evolutionary groups of enzymes, bacterial and methanogenic. These two types of SerRSs display only minimal sequence similarity, primarily within the class II conserved motifs, and possess distinct modes of tRNA(Ser) recognition. In order

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.

J Sélambarom et al.

Carbohydrate research, 330(1), 43-51 (2001-02-24)

The reaction of L-serine methyl ester hydrochloride (1) with paraformaldehyde (2) in dichloromethane in the presence of triethylamine afforded a novel compound: [lS,2S,6S,7S]-1,6-diaza-4,9-dioxa-2,7-dimethoxycarbonylbicyclo[4.4.1]undecane (4) as a 2:3 adduct of 1 with 2. 1H and 13C NMR spectroscopy were unable to

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Global Trade Item Number

SKU	GTIN
223131-10G	04061832641867
223131-100G	04061832641850