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质量水平
方案
≥95%
表单
powder or crystals
反应适用性
reaction type: click chemistry
储存温度
−20°C
SMILES字符串
[Si](C)(C)(C)C#Cc1cc(cc(c1)Br)[S](=O)(=O)F
InChI
1S/C11H12BrFO2SSi/c1-17(2,3)5-4-9-6-10(12)8-11(7-9)16(13,14)15/h6-8H,1-3H3
InChI key
CUUVPHAGWQDSCZ-UHFFFAOYSA-N
应用
3-Bromo-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.
相关产品
产品编号
说明
价格
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
商品
In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.
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