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410209

Sigma-Aldrich

L-Cysteinmethylester -hydrochlorid

98%

Synonym(e):

(R)-Cysteine methyl ester hydrochloride

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About This Item

Lineare Formel:
HSCH2CH(NH2)COOCH3 · HCl
CAS-Nummer:
18598-63-5
Molekulargewicht:
171.65
Beilstein:
3685824
EG-Nummer:
242-435-0
MDL-Nummer:
MFCD00038985
UNSPSC-Code:
12352209
eCl@ss:
32160406
PubChem Substanz-ID:
24865699
NACRES:
NA.22

Qualitätsniveau

100

Assay

98%

Form

solid

Optische Aktivität

[α]20/D −1.8°, c = 10 in methanol

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

142 °C (dec.) (lit.)

Anwendung(en)

peptide synthesis

SMILES String

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

InChI

1S/C4H9NO2S.ClH/c1-7-4(6)3(5)2-8;/h3,8H,2,5H2,1H3;1H/t3-;/m0./s1

InChIKey

WHOHXJZQBJXAKL-DFWYDOINSA-N

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Verwandte Kategorien

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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L-Cystein 97%

Sigma-Aldrich

168149

L-Cystein

(R)-(+)-Cysteine for synthesis

Sigma-Aldrich

8.16014

(R)-(+)-Cysteine

H Yin et al.
Chemical research in toxicology, 9(1), 140-146 (1996-01-01)
Trihaloacetaldehydes are used as sedatives, are key intermediates in the metabolism of 1,1,1,2-tetrahaloethanes, some of which are chlorofluorocarbon substitutes, and are metabolites of trihaloethanols, which are intestinal and bone marrow toxins. In the present study, trifluoroacetaldehyde was used as a
B E Svensson
The Biochemical journal, 253(2), 441-449 (1988-07-15)
Nine low-Mr thiols were compared with regard to their ability to function as myeloperoxidase-oxidase substrates under conditions where no auto-oxidation of the thiols could be observed. The methyl and ethyl esters of cysteine were found to be about twice as
M Yoshikuni et al.
Developmental biology, 128(1), 236-239 (1988-07-01)
Several disulfide-reducing agents, such as dithiothreitol, 2,3-dimercapto-1-propanol, cysteine ethyl ester, and cysteine methyl ester enhanced the effectiveness of 1-methyladenine (1-MeAde) to induce oocyte maturation in the starfish Asterina pectinifera. This enhancement occurred at relatively low concentrations at which these agents
T A Cook et al.
Biochemistry, 39(44), 13516-13523 (2000-11-07)
PDE6 (type 6 phosphodiesterase) from rod outer segments consists of two types of catalytic subunits, alpha and beta; two inhibitory gamma subunits; and one or more delta subunits found only on the soluble form of the enzyme. About 70% of
Mickael Alimi et al.
Inorganic chemistry, 51(17), 9350-9356 (2012-08-22)
Six Co(III) complexes based on unsubstituted or substituted TPA ligands (where TPA is tris(2-pyridylmethyl)amine) and acetohydroxamic acid (A), N-methyl-acetohydroxamic acid (B), or N-hydroxy-pyridinone (C) were prepared and characterized by mass spectrometry, elemental analysis, and electrochemistry: [Co(III)(TPA)(A-2H)](Cl) (1a), [Co(III)((4-Cl(2))TPA)(A-2H)](Cl) (2a), [Co(III)((6-Piva)TPA)(A-2H)](Cl)
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