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Merck
CN

900865

4-Formyl-2-((trimethylsilyl)ethynyl)benzenesulfonyl fluoride

≥95%

别名:

Formyl sulfonyl fluoride TMS-Alkyne, Probe building block

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关于此项目

经验公式(希尔记法):
C12H13FO3SSi
化学文摘社编号:
分子量:
284.38
UNSPSC Code:
12352200
NACRES:
NA.22
Assay:
≥95%
Form:
powder or crystals
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assay

≥95%

form

powder or crystals

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

SMILES string

O=CC1=CC=C(S(=O)(F)=O)C(C#C[Si](C)(C)C)=C1

Application

4-Formyl-2-((trimethylsilyl)ethynyl)benzenesulfonyl fluoride is used for chemical probe synthesis, this trifunctional building block contains an aryl sulfonyl fluoride group, alkyne tag, and aldehyde synthetic handle. When appended to a ligand or pharmacophore through its formyl linker, this building block allows for SuFEx-enabled, context-specific covalent modification of a biological target with potential for downstream applications via the alkyne tag. Use alone or in parallel with other multi-functional building blocks to discover the optimal probe for your chemical biology experiments.


存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

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商品

在与K. Barry Sharpless及其同事合作后,Sigma-Aldrich现可提供各种磺酰氟试剂,这些试剂经历了“Click II”反应。

In collaboration with K. Barry Sharpless and coworkers, we offer a variety of sulfonyl fluoride reagents that undergo a “Click II” reaction.

In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.





全球贸易项目编号

货号GTIN
900865-50MG04061833251317