791040
Zinc n-propylsulfinate
95% (H-NMR)
别名:
Baran NPS Reagent, Bis[(propylsulfinyl)oxy]zinc
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关于此项目
经验公式（希尔记法）:
C6H14O4S2Zn
化学文摘社编号:
分子量:
279.69
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
Assay:
95% (H-NMR)
Form:
solid
SMILES string
CCCS(O[Zn]OS(CCC)=O)=O
InChI
1S/2C3H8O2S.Zn/c2*1-2-3-6(4)5;/h2*2-3H2,1H3,(H,4,5);/q;;+2/p-2
InChI key
AVEWLRYVGNMIHD-UHFFFAOYSA-L
assay
95% (H-NMR)
form
solid
reaction suitability
reaction type: C-C Bond Formation, reagent type: catalyst
reaction type: C-H Activation
mp
80-105 °C
functional group
sulfinic acid
storage temp.
2-8°C
Application
Zinc n-propylsulfinate (NPS) is part of a zinc sulfinate toolbox developed by Phil Baran for the simple and rapid diversification of heterocycles.
Learn More at the Professor and Product Portal of Professor Phil S. Baran.
Practical and Innate Carbon-Hydrogen Functionalization of Heterocycles
Learn More at the Professor and Product Portal of Professor Phil S. Baran.
Practical and Innate Carbon-Hydrogen Functionalization of Heterocycles
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Fionn O'Hara et al.
Journal of the American Chemical Society, 135(32), 12122-12134 (2013-07-19)
Radical addition processes can be ideally suited for the direct functionalization of heteroaromatic bases, yet these processes are only sparsely used due to the perception of poor or unreliable control of regiochemistry. A systematic investigation of factors affecting the regiochemistry
Yuta Fujiwara et al.
Nature, 492(7427), 95-99 (2012-12-04)
Nitrogen-rich heterocyclic compounds have had a profound effect on human health because these chemical motifs are found in a large number of drugs used to combat a broad range of diseases and pathophysiological conditions. Advances in transition-metal-mediated cross-coupling have simplified
商品
Rapidly diversify (hetero)aromatic scaffolds for chemical industry needs amid resource and time constraints, ensuring efficiency.
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