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Merck
CN

900605

3-(Bromomethyl)-5-((trimethylsilyl)ethynyl)benzenesulfonyl fluoride

≥95%

别名:

Bromo sulfonyl fluoride alkyne, Probe building block

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关于此项目

经验公式(希尔记法):
C12H14BrFO2SSi
化学文摘社编号:
分子量:
349.29
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.22
Assay:
≥95%
Form:
solid
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Quality Level

assay

≥95%

form

solid

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

SMILES string

[Si](C)(C)(C)C#Cc1cc(cc(c1)CBr)[S](=O)(=O)F

InChI

1S/C12H14BrFO2SSi/c1-18(2,3)5-4-10-6-11(9-13)8-12(7-10)17(14,15)16/h6-8H,9H2,1-3H3

InChI key

QSYGHPYMWBAJRL-UHFFFAOYSA-N

Application

3-(Bromomethyl)-5-((trimethylsilyl)ethynyl)benzenesulfonyl fluoride is used for chemical probe synthesis, this trifunctional building block contains an aryl sulfonyl fluoride group, alkyne tag, and bromine synthetic handle. When appended to a ligand or pharmacophore through its brominated 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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

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商品

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
900605-100MG04061833250488