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Merck

730416

Sigma-Aldrich

S-(α-Fluorobenzyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximine

97%

别名:

N-[(fluorophenylmethyl)oxidophenyl-λ4-sulfanylidene]-4-methyl-benzenesulfonamide

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About This Item

经验公式(希尔记法):
C20H18FNO3S2
分子量:
403.49
MDL號碼:
分類程式碼代碼:
12352101
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

solid

mp

148-154 °C

SMILES 字串

Cc1ccc(cc1)S(=O)(=O)N=S(=O)(C(F)c2ccccc2)c3ccccc3

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

InChI 密鑰

ZAGQEXRRSCLLFW-UHFFFAOYSA-N

應用

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.

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

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 and catalysis, 352(16), 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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