V900635
2-巯基吡啶
Vetec™, reagent grade, 98%
别名:
2-吡啶硫醇, 2-硫吡啶
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关于此项目
经验公式（希尔记法）:
C5H5NS
化学文摘社编号:
分子量:
111.16
EC Number:
220-131-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
105787
MDL number:
Assay:
98%
InChI key
WHMDPDGBKYUEMW-UHFFFAOYSA-N
InChI
1S/C5H5NS/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)
SMILES string
Sc1ccccn1
grade
reagent grade
product line
Vetec™
assay
98%
storage temp.
2-8°C
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Sasa Koncarevic et al.
Free radical biology & medicine, 46(8), 1096-1108 (2009-05-15)
Terpyridineplatinum(II) complexes (TPCs) efficiently inhibit the proliferation of glioblastoma cells in vitro and have been tested successfully in a rodent glioblastoma model. Apart from intercalation with DNA, the major mechanism of action of TPCs is a very potent and specific
Gavin Dyson et al.
Dalton transactions (Cambridge, England : 2003), (31)(31), 6120-6126 (2010-05-08)
A new family of flexible scorpionate ligands based on 2-mercaptopyridine is reported. The tris- and bis-substituted ligands, K[HB(mp)(3)] (1) and Na[H(2)B(mp)(2)] (2) (mp = 2-mercaptopyridine) have been prepared and fully characterised. The structural characterisation of 1 reveals an unprecedented mu(3)-kappa(3)-SS'H-eta(1)eta(1)eta(2)-kappa(2)-S''C-eta(1)eta(1)-kappa(1)-S'-eta(1)
Xavier Roussel et al.
The Journal of biological chemistry, 284(48), 33048-33055 (2009-10-06)
Sulfiredoxin catalyzes the ATP-dependent reduction of overoxidized eukaryotic 2-Cys peroxiredoxin PrxSO(2) into sulfenic PrxSOH. Recent mechanistic studies on sulfiredoxins have validated a catalytic mechanism that includes formation of a phosphoryl intermediate on the sulfinyl moiety of PrxSO(2), followed by an
Partha Halder et al.
Inorganic chemistry, 50(3), 708-710 (2010-12-25)
Iron(II) tris(2-pyridylthio)methanido (1) containing an Fe-C bond, obtained from the reaction of tris(2-pyridylthio)methane (HL(1)) and iron(II) triflate, reacts with protic acid to generate iron(II) bis(2-pyridylthio)carbene (1a). The carbene complex is converted to an iron(II) complex (2) of the 1-[bis(2-pyridylthio)methyl]pyridine-2-thione ligand
H I Abdulla et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(13), 2659-2671 (2002-01-05)
The infrared spectra of 2-hydroxypyridine (2-OHP), 2-thiopyridine (2-SHP), and 2-aminopyridine (2-NH2P) have been recorded in the solid, liquid and vapor phases in the region 4000-200 cm(-1). To support the work, deuterated forms of these compounds in the functional groups XH
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