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化驗
≥95%
形狀
solid
反應適用性
reaction type: click chemistry
儲存溫度
−20°C
SMILES 字串
O=C([H])C1=CC(S(=O)(F)=O)=CC(C#C[Si](C)(C)C)=C1
應用
3-Formyl-5-((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 group, 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.
相關產品
产品编号
说明
价格
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
商品
In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.
In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.
In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.
In partnership with Pfizer chemists, we have compiled a collection of trifunctional building blocks to enable development of probes.
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