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Merck
CN

900862

(4-(3-(Trifluoromethyl)-3H-diazirin-3-yl)-2-((trimethylsilyl)ethynyl)phenyl)methanol

别名:

Hydroxyl diazirine TMS-alkyne, Probe building block

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关于此项目

经验公式(希尔记法):
C14H15F3N2OSi
化学文摘社编号:
分子量:
312.36
UNSPSC Code:
12352200
NACRES:
NA.22
Assay:
≥95%
Form:
powder or crystals
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SMILES string

OCC1=CC=C(C2(N=N2)C(F)(F)F)C=C1C#C[Si](C)(C)C

assay

≥95%

form

powder or crystals

storage temp.

−20°C

Application

(4-(3-(Trifluoromethyl)-3H-diazirin-3-yl)-2-((trimethylsilyl)ethynyl)phenyl)methanol is used for chemical probe synthesis, this trifunctional building block contains a light-activated diazirine, alkyne tag, and hydroxyl synthetic handle. When appended to a ligand or pharmacophore through its hydroxyl linker, this building block allows for UV light-induced 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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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

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