730416
S-(α-Fluorobenzyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximine
97%
别名:
N-[(fluorophenylmethyl)oxidophenyl-λ4-sulfanylidene]-4-methyl-benzenesulfonamide
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关于此项目
经验公式（希尔记法）:
C20H18FNO3S2
化学文摘社编号:
分子量:
403.49
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
Assay:
97%
Form:
solid
InChI
1S/C20H18FNO3S2/c1-16-12-14-19(15-13-16)27(24,25)22-26(23,18-10-6-3-7-11-18)20(21)17-8-4-2-5-9-17/h2-15,20H,1H3
SMILES string
Cc1ccc(cc1)S(=O)(=O)N=S(=O)(C(F)c2ccccc2)c3ccccc3
InChI key
ZAGQEXRRSCLLFW-UHFFFAOYSA-N
assay
97%
form
solid
mp
148-154 °C
Application
S-(α-Fluorobenzyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximine can be used as a reagent for the synthesis of monofluorinated epoxides byO-cyclization reaction with ketones in the presence of a strong base.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Efficient Synthesis and Ring-Opening Reactions of Monofluorinated Epoxides Derived from α-Fluorosulfoximines
Zhang W and Hu J
advanced synthesis and catalysis, 352(16), 2799-2804 (2010)
Efficient Synthesis and Ring-Opening Reactions of Monofluorinated Epoxides Derived from a-Fluorosulfoximines
Zhang, W.; Hu, J.
Advanced Synthesis & Catalysis, 352, 2799-2804 (2010)
Efficient Synthesis and Ring-Opening Reactions of Monofluorinated Epoxides Derived from α-Fluorosulfoximines
Zhang W and Hu J
Advanced Synthesis & Catalysis, 352(16), 2799-2804 (2010)
相关内容
Prof. Jinbo Hu's lab focuses on developing new fluorination reagents and reactions, including difluoromethylation and monofluoromethylation.
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