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Merck
CN

900602

4-(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
UNSPSC Code:
12352106
NACRES:
NA.22
MDL number:
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产品名称

4-(4-(Prop-2-yn-1-yloxy)benzoyl)benzoic acid, ≥95%

InChI

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

SMILES string

O=C(C1=CC=C(OCC#C)C=C1)C2=CC=C(C(O)=O)C=C2

InChI key

URDMKFAPEKSQDV-UHFFFAOYSA-N

assay

≥95%

form

solid

reaction suitability

reaction type: click chemistry
reagent type: cross-linking reagent

functional group

alkyne
carboxylic acid

storage temp.

−20°C

Quality Level

Application

4-(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.

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)

Lot/Batch Number

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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.

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