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Merck
CN

900615

(4-Hydroxyphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone

≥95%

别名:

Hydroxyl benzophenone alkyne, Probe building block

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关于此项目

经验公式(希尔记法):
C16H12O3
化学文摘社编号:
分子量:
252.26
UNSPSC Code:
12352200
NACRES:
NA.22
MDL number:
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

O(CC#C)c1ccc(cc1)C(=O)c2ccc(cc2)O

InChI

1S/C16H12O3/c1-2-11-19-15-9-5-13(6-10-15)16(18)12-3-7-14(17)8-4-12/h1,3-10,17H,11H2

InChI key

TZKIHDJSIXVMIQ-UHFFFAOYSA-N

Application

(4-Hydroxyphenyl)(4-(prop-2-yn-1-yloxy)phenyl)methanone is used for chemical probe synthesis, this trifunctional building block contains a light-activated benzophenone, 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

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
C9373-25MG04061832897738
C9373-5MG04061832897745
900615-100MG04061833250556