412201
L-Serine methyl ester hydrochloride
98%, for peptide synthesis
Synonym(s):
L-Serine methyl ester·HCl
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About This Item
Linear Formula:
HOCH2CH(NH2)COOCH3 · HCl
CAS Number:
Molecular Weight:
155.58
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
227-140-7
MDL number:
Beilstein/REAXYS Number:
3559591
Product Name
L-Serine methyl ester hydrochloride, 98%
Quality Level
assay
98%
form
powder
optical activity
[α]20/D +3.4°, c = 4 in methanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
163 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
Cl.COC(=O)[C@@H](N)CO
InChI
1S/C4H9NO3.ClH/c1-8-4(7)3(5)2-6;/h3,6H,2,5H2,1H3;1H/t3-;/m0./s1
InChI key
NDBQJIBNNUJNHA-DFWYDOINSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
Yu Harayama et al.
Chemical communications (Cambridge, England), (13)(13), 1764-1766 (2005-03-26)
The use of hypervalent iodine(III) reagents allowed us to develop the novel and efficient direct synthesis of N,O-acetal compounds via the oxidative fragmentation reaction of alpha-amino acids or alpha-amino alcohols; furthermore, we succeeded in developing an improved synthesis of the
Ernest Mordret et al.
Molecular cell, 75(3), 427-441 (2019-07-30)
The translation machinery and the genes it decodes co-evolved to achieve production throughput and accuracy. Nonetheless, translation errors are frequent, and they affect physiology and protein evolution. Mapping translation errors in proteomes and understanding their causes is hindered by lack