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

ALDRICH/900602 - ≥95%

Synonym: Carboxyl benzophenone alkyne; Probe building block

CAS Number: 1236196-77-2
Empirical Formula (Hill Notation): C₁₇H₁₂O₄
Molecular Weight: 280.27
MDL Number: MFCD21648478
Linear Formula: C₁₇H₁₂O₄
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-900602-100MG	100 mg	$275.00 1/EAAdd To Favorites		Add To Favorites

assay	≥95%
form	solid
functional group	alkyne
	carboxylic acid
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
Quality Level	100
reaction suitability	reaction type: click chemistry
	reagent type: cross-linking reagent
SMILES string	O=C(C1=CC=C(OCC#C)C=C1)C2=CC=C(C(O)=O)C=C2
storage temp.	−20°C

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:	Technology Spotlight: Trifuctional Probe Building Blocks A library approach to rapidly discover photoaffinity probes of the mRNA decapping scavenger enzyme DcpS Synthesis and Evaluation of New Thiodigalactoside-Based Chemical Probes to Label Galectin-3 Discovery of tumor-specific irreversible inhibitors of stearoyl CoA desaturase
Packaging:	100 mg in glass bottle