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Merck
CN

ALD00170

1，2-苯二磺酰氟

97%

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关于此项目

经验公式（希尔记法）:
C6H4F2O4S2
化学文摘社编号:
115560-96-8
分子量:
242.22
MDL number:
MFCD28963805
UNSPSC Code:
12352100
PubChem Substance ID:
329772621
NACRES:
NA.22
Assay:
97%
Form:
solid

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产品名称

1，2-苯二磺酰氟, 97%

SMILES string

O=S(C1=C(S(=O)(F)=O)C=CC=C1)(F)=O

InChI

1S/C6H4F2O4S2/c7-13(9,10)5-3-1-2-4-6(5)14(8,11)12/h1-4H

InChI key

DNXLZBKMVRTNHQ-UHFFFAOYSA-N

assay

97%

form

solid

reaction suitability

reaction type: click chemistry

mp

127-132 °C

Quality Level

100

相关类别

Application

Sulfonyl fluoride motif can be used as a connector for the assembly of -SO2- linked small molecules with proteins or nucleic acids. This new click chemistry approach through sulfates is a complimentary approach to using amides and phosphate groups as linkers.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKBT7554V

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商品

Recent Advances in the Catalytic Transformations

This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.

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Sharpless Group – Professor Product Portal

The Sharpless Lab pursues useful new reactivity and general methods for selectively controlling chemical reactions.

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