10425-11-3 | 3,4-Dihydroxybenzophenone

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$25.00	$17.00
10g	95%	in stock	$28.00	$19.00
25g	95%	in stock	$40.00	$28.00
100g	95%	in stock	$129.00	$90.00
500g	95%	in stock	$440.00	$308.00

Description

• Catalog Number: AB63732
• Chemical Name: 3,4-Dihydroxybenzophenone
• CAS Number: 10425-11-3
• Molecular Formula: C13H10O3
• Molecular Weight: 214.2167
• MDL Number: MFCD29919416
• SMILES: O=C(c1ccc(c(c1)O)O)c1ccccc1

Computed Properties

• Complexity: 246
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: 2.6

Upstream Synthesis Route

The compound (3,4-Dihydroxyphenyl)(phenyl)methanone, also known as hydroxyacetophenone, plays a crucial role in chemical synthesis as a versatile building block and reagent. With its unique structure combining a phenolic group and a ketone group, this compound is utilized in various synthetic pathways to create a diverse range of organic molecules.In chemical synthesis, (3,4-Dihydroxyphenyl)(phenyl)methanone serves as a key intermediate for the construction of more complex compounds. Its functional groups enable it to participate in a variety of chemical reactions, including nucleophilic substitution, oxidation, and reduction reactions. By selectively modifying the phenolic or ketonic moieties, chemists can tailor the molecular structure and properties of the final product.Furthermore, (3,4-Dihydroxyphenyl)(phenyl)methanone is often employed in the synthesis of pharmaceuticals, dyes, perfumes, and natural products. Its ability to undergo diverse transformations makes it a valuable tool for creating new chemical entities with specific biological activities or desirable characteristics.Overall, the application of (3,4-Dihydroxyphenyl)(phenyl)methanone in chemical synthesis showcases its significance in enabling the efficient and controlled construction of organic molecules with tailored functionalities and applications.

Literature

• Pseudopolymorphism in hydroxybenzophenones: the dihydrate of 2,2',4,4'-tetrahydroxybenzophenone.

  Acta crystallographica. Section C, Crystal structure communications 20120401

• Small molecule AKAP-protein kinase A (PKA) interaction disruptors that activate PKA interfere with compartmentalized cAMP signaling in cardiac myocytes.

  The Journal of biological chemistry 20110318

• A monohydrate pseudopolymorph of 3,4-dihydroxybenzophenone and the role of water in the crystal assembly of benzophenones.

  Acta crystallographica. Section C, Crystal structure communications 20100901