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Merck
CN

900614

3-(4-(Prop-2-yn-1-yloxy)benzoyl)benzoic 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):
C17H12O4
化学文摘社编号:
分子量:
280.27
MDL number:
UNSPSC Code:
12352106
NACRES:
NA.22
Assay:
≥95%
Form:
solid
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InChI

1S/C17H12O4/c1-2-10-21-15-8-6-12(7-9-15)16(18)13-4-3-5-14(11-13)17(19)20/h1,3-9,11H,10H2,(H,19,20)

InChI key

ZQWRDUVGHBGHPV-UHFFFAOYSA-N

SMILES string

O(CC#C)c1ccc(cc1)C(=O)c2cc(ccc2)C(=O)O

assay

≥95%

form

solid

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

Quality Level

Application

3-(4-(Prop-2-yn-1-yloxy)benzoyl)benzoic 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

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

法规信息

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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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