410209
L-半胱氨酸甲酯 盐酸盐
98%, for peptide synthesis
别名:
(R)-Cysteine methyl ester hydrochloride
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关于此项目
线性分子式:
HSCH2CH(NH2)COOCH3 · HCl
化学文摘社编号:
分子量:
171.65
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
242-435-0
MDL number:
Beilstein/REAXYS Number:
3685824
产品名称
L-半胱氨酸甲酯 盐酸盐, 98%
InChI key
WHOHXJZQBJXAKL-DFWYDOINSA-N
InChI
1S/C4H9NO2S.ClH/c1-7-4(6)3(5)2-8;/h3,8H,2,5H2,1H3;1H/t3-;/m0./s1
SMILES string
Cl[H].COC(=O)[C@@H](N)CS
assay
98%
form
solid
optical activity
[α]20/D −1.8°, c = 10 in methanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
142 °C (dec.) (lit.)
application(s)
peptide synthesis
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
A F Lailey et al.
Biochemical pharmacology, 42 Suppl, S47-S54 (1991-12-11)
Perfluoroisobutene (PFIB) is a hydrophobic reactive gas produced by the pyrolysis of polytetrafluoroethane which induces pulmonary oedema similar to that induced by phosgene when inhaled. When a lethal dose is inhaled by Porton strain rats total non-protein thiol (NPSH) and
Mohamed R Shehata et al.
Dalton transactions (Cambridge, England : 2003), (6)(6), 779-786 (2008-02-02)
The complex-formation equilibria of [Pd(SMC)(H2O)2]+, where SMC = S-methyl-l-cysteinate, with bio-relevant ligands such as amino acids, peptides, dicarboxylic acids and DNA constituents were studied and their formation constants were determined. The binding mode of the ligands containing various functional groups
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
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
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