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关于此项目
经验公式(希尔记法):
C5H4NNaO2S
化学文摘社编号:
分子量:
165.15
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.22
form
powder or crystals
Quality Segment
reaction suitability
reaction type: C-C Bond Formation
mp
292 °C
functional group
sulfinic acid
SMILES string
[Na+].[S](=O)([O-])c1ncccc1
InChI
1S/C5H5NO2S.Na/c7-9(8)5-3-1-2-4-6-5;/h1-4H,(H,7,8);/q;+1/p-1
InChI key
HQCGASCBCQJRDJ-UHFFFAOYSA-M
Application
This 2-pyridylsulfinate enables Suzuki-Miyaura cross coupling with aryl halides to access diverse pyridine derivatives as reported by the laboratory of Michael Willis.. No longer impeded by unstable 2-pyridyl boronates, the sulfinate alternatives provide Pd-catalyzed coupling routes to therapeutically valuable pyridine rings.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
