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Merck
CN

900602

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

≥95%

Synonym(s):

Carboxyl benzophenone alkyne, Probe building block

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About This Item

Empirical Formula (Hill Notation):
C17H12O4
CAS Number:
1236196-77-2
Molecular Weight:
280.27
UNSPSC Code:
12352106
NACRES:
NA.22
MDL number:
MFCD21648478

Key Documents

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Product Name

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

100

Related Categories

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.

Other Notes


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX3695
MKCM7607

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Articles

Trifunctional Probe Building Blocks

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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