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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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-131-9
Beilstein/REAXYS Number:
105787
MDL number:
产品名称
2-巯基吡啶, ReagentPlus®, 99%
InChI key
WHMDPDGBKYUEMW-UHFFFAOYSA-N
InChI
1S/C5H5NS/c7-5-3-1-2-4-6-5/h1-4H,(H,6,7)
SMILES string
Sc1ccccn1
product line
ReagentPlus®
assay
99%
mp
127-130 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
用作金属络合物中的配体。
General description
2-巯基吡啶是有机硫化物,含有不止一个杂原子。常用作各种有机合成反应的亲核体,并因为π-酸性在配位化学中发挥重要的多功能配体作用。
Legal Information
ReagentPlus is a registered 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
ppe
dust mask type N95 (US), Eyeshields, Gloves
Elucidating the adsorption of 2-Mercaptopyridine drug on the aluminum phosphide (Al12P12) nanocage: A DFT study
Al-shimaa R SM, et al.
Heliyon, 9 (2023)
Synthesis and Structure of Weta2-mp) 2 (CO) 3 (mp= Monoanion of 2-Mercaptopyridine) and Its Reactions with 2, 2 `-Pyridine Disulfide and/or NO To Yield Weta 2-mp) 4, Weta 2-mp) 2 (NO) 2, and Weta 2-mp) 3 (NO)},
Kengkaj S, et al.
Inorganic Chemistry, 40, 2402-2408 (2001)
A new facile electrochemical method for the synthesis of 4-(pyridine-2-ylthio) benzene-l, 2-diols
Mojtaba S, et al.
Electrochimica Acta, 51, 3327-3331 (2006)
Inorganic Chemistry, 33, 5167-5167 (1994)
Étienne Rochette et al.
Journal of the American Chemical Society, 141(31), 12305-12311 (2019-07-10)
The potential advantages of using arylboronic esters as boron sources in C-H borylation are discussed. The concept is showcased using commercially available 2-mercaptopyridine as a metal-free catalyst for the transfer borylation of heteroarenes using arylboronates as borylation agents. The catalysis
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