FluoroMethyl 2-pyridyl sulfone

FluoroMethyl 2-pyridyl sulfone Suppliers list
Company Name: Allfluoro pharmaceutical co. ltd.
Tel: 021-26137118 +8615821363818
Email: sales@allfluoro.com
Products Intro: Product Name:Fluoromethyl 2-pyridylsulfone
CAS:1365765-53-2
Purity:0.98 Package:1KG;10KG;100KG;1000KG
Company Name: ANHUI WITOP BIOTECH CO., LTD
Tel: +8615255079626
Email: eric@witopchemical.com
Products Intro: Product Name:FluoroMethyl 2-pyridyl sulfone
CAS:1365765-53-2
Company Name: Henan Alfa Chemical Co., Ltd
Tel: +8618339805032
Email: alfa4@alfachem.cn
Products Intro: CAS:1365765-53-2
Purity:97%+ Package:5g; 25g; 100g; 500g; 1kg; 25kg
Company Name: Sichuan Biosynce Pharmatech Co., Ltd.
Tel: +8619950309693
Email: diane@biosynce.com
Products Intro: Product Name:Fluoromethyl 2-pyridyl sulfone
CAS:1365765-53-2
Purity:0.95_) Package:10G;50G;100G Remarks:Chemically Pure
Company Name: Shanxi Tihondan Pharmaceutical Technology Co., Ltd
Tel: +8618235132063
Email: sales@tihondan.com
Products Intro: Product Name:2-((fluoromethyl)sulfonyl)pyridine
CAS:1365765-53-2
Purity:95%+ Package:5g;10g;1kg;10kg

FluoroMethyl 2-pyridyl sulfone manufacturers

FluoroMethyl 2-pyridyl sulfone Basic information
Product Name:FluoroMethyl 2-pyridyl sulfone
Synonyms:FluoroMethyl 2-pyridyl sulfone;2-[(Fluoromethyl)sulfonyl]-pyridine;Pyridine, 2-[(fluoromethyl)sulfonyl]-;FM-2-pyridyl sulfone;2-Pyridyl fluoromethyl sulfone;Pyridine, 2-[(fluoromethyl)sulfonyl]-2-fluoromethanesulfonylpyridine
CAS:1365765-53-2
MF:C6H6FNO2S
MW:175.18
EINECS:
Product Categories:
Mol File:1365765-53-2.mol
FluoroMethyl 2-pyridyl sulfone Structure
FluoroMethyl 2-pyridyl sulfone Chemical Properties
Boiling point 353.2±35.0 °C(Predicted)
density 1.348±0.06 g/cm3(Predicted)
pka-3.04±0.19(Predicted)
Safety Information
Safety Statements 24/25
HS Code 29309090
MSDS Information
FluoroMethyl 2-pyridyl sulfone Usage And Synthesis
Description Fluoromethyl 2-pyridyl sulfone and its derivatives can be used as novel monofluoromethylation reagents. The monofluorinated sulfinate intermediates during the monofluoroolefination of aldehydes and ketones can be halogenated in situ to afford mono- and dihalofluoroalkyl compounds. The coupling reaction between iodofluoromethyl 2-pyridyl sulfone and aryl iodides mediated by copper can be used to prepare monofluoromethyl arenes and heteroarenes.
Chemical Propertieswhite solid
Reactions(1) Dihalofluoromethylation of aldehydes and ketones.
FluoroMethyl 2-pyridyl sulfone(2) Halofluoroalkylation of aldehydes.
FluoroMethyl 2-pyridyl sulfone
(3) Monofluoromethylation of arenes and heteroarenes.
FluoroMethyl 2-pyridyl sulfone
References[1] YANCHUAN ZHAO Jinbo H Bing Gao. From Olefination to Alkylation: In-Situ Halogenation of Julia–Kocienski Intermediates Leading to Formal Nucleophilic Iodo- and Bromodifluoromethylation of Carbonyl Compounds[J]. Journal of the American Chemical Society, 2012, 134 13: 5790-5793. DOI:10.1021/ja301601b.
[2] YANCHUAN ZHAO. Copper-Mediated Fluoroalkylation of Aryl Iodides Enables Facile Access to Diverse Fluorinated Compounds: The Important Role of the (2-Pyridyl)sulfonyl Group[J]. Organic Letters, 2012, 14 23: 6080-6083. DOI:10.1021/ol3029737.
FluoroMethyl 2-pyridyl sulfone Preparation Products And Raw materials
Tag:FluoroMethyl 2-pyridyl sulfone(1365765-53-2) Related Product Information
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