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Merck
CN

900613

5-(4-(4-(Prop-2-yn-1-yloxy)benzoyl)phenoxy)pentanoic acid

≥95%

别名:

Carboxyl benzophenone alkyne, Probe building block

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关于此项目

经验公式(希尔记法):
C21H20O5
化学文摘社编号:
分子量:
352.38
MDL number:
UNSPSC Code:
12352106
NACRES:
NA.22
Assay:
≥95%
Form:
solid
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InChI key

PVDBYWSDYKTIBJ-UHFFFAOYSA-N

InChI

1S/C21H20O5/c1-2-14-25-18-10-6-16(7-11-18)21(24)17-8-12-19(13-9-17)26-15-4-3-5-20(22)23/h1,6-13H,3-5,14-15H2,(H,22,23)

SMILES string

O(CCCCC(=O)O)c1ccc(cc1)C(=O)c2ccc(cc2)OCC#C

assay

≥95%

form

solid

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

Quality Level

Application

5-(4-(4-(Prop-2-yn-1-yloxy)benzoyl)phenoxy)pentanoic acid is used for chemical probe synthesis, this trifunctional building block contains a light-activated benzophenone, alkyne tag, and carboxylic acid synthetic handle. When appended to a ligand or pharmacophore through its acid 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.

pictograms

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signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

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

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