67787
N-(Methyl)mercaptoacetamide
≥97.0% (RT)
Synonim(y):
N-(Methyl)thioglycolamide
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Informacje o tej pozycji
Wzór liniowy:
HSCH2CONHCH3
Numer CAS:
Masa cząsteczkowa:
105.16
UNSPSC Code:
12352200
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1740652
Przejdź do
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Pozwól nam pomócInChI
1S/C3H7NOS/c1-4-3(5)2-6/h6H,2H2,1H3,(H,4,5)
SMILES string
CNC(=O)CS
InChI key
NSJNRJYQQPRCLF-UHFFFAOYSA-N
assay
≥97.0% (RT)
refractive index
n20/D 1.523
bp
83-85 °C/0.3 mmHg
density
1.19 g/mL at 20 °C (lit.)
storage temp.
2-8°C
Application
N-(Methyl)mercaptoacetamide is a reducing agent that reacts with methionine sulfoxide moieties. N-(Methyl)mercaptoacetamide may be used as a reference material in assays wherein this molecule is an expected leaving group. N-(Methyl)mercaptoacetamide is used in various zinc complexes to study metalloprotein structure and interactions.
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
R.I. Lundblad et al.
Chemical Reagents for Protein Modification, I, 99-99 (1984)
David T Puerta et al.
Inorganic chemistry, 41(20), 5075-5082 (2002-10-02)
The tetrahedral zinc complex [(Tp(Me,Ph))ZnOH] (Tp(Me,Ph) = hydrotris(5,3-methylphenylpyrazolyl)borate) was combined with acetohydroxamic acid, 3-mercapto-2-butanone, N-(methyl)mercaptoacetamide, beta-mercaptoethanol, 3-mercapto-2-propanol, and 3-mercapto-2-butanol to generate the complexes [(Tp(Me,Ph))Zn(ZBG)] (ZBG = zinc-binding group). These complexes were prepared to determine the mode of binding for three
Isolation and biochemical characterization of a novel lantibiotic mutacin from Streptococcus mutans.
J Novák et al.
Journal of bacteriology, 176(14), 4316-4320 (1994-07-01)
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Peter Eyer et al.
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