Skip to Content
Merck
CN

900602

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

≥95%

Synonym(s):

Carboxyl benzophenone alkyne, Probe building block

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C17H12O4
CAS Number:
Molecular Weight:
280.27
UNSPSC Code:
12352106
NACRES:
NA.22
MDL number:
Assay:
≥95%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Segment

assay

≥95%

form

solid

reaction suitability

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

functional group

alkyne, carboxylic acid

storage temp.

−20°C

SMILES string

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

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)

InChI key

URDMKFAPEKSQDV-UHFFFAOYSA-N

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.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library