900602

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

≥95%

• Synonyme(s) : Carboxyl benzophenone alkyne, Probe building block
• Formule empirique (notation de Hill): C₁₇H₁₂O₄
• Numéro CAS: 1236196-77-2
• Poids moléculaire : 280.27
• Numéro MDL: MFCD21648478
• Code UNSPSC : 12352106
• Nomenclature NACRES : NA.22

Propriétés

• Niveau de qualité: 100
• Pureté: ≥95%
• Forme: solid
• Capacité de réaction: reaction type: click chemistry
• Pertinence de la réaction: reagent type: cross-linking reagent
• Groupe fonctionnel: alkyne; carboxylic acid
• Température de stockage: −20°C
• Chaîne SMILES: 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)
• Clé InChI: URDMKFAPEKSQDV-UHFFFAOYSA-N

Description

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.

Autres remarques

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Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable