10345-87-6 | 3-Phenylcyclohex-2-en-1-one

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$131.00	$92.00
1g	98%	in stock	$325.00	$228.00
5g	98%	in stock	$946.00	$662.00
10g	98%	in stock	$1,412.00	$989.00

Description

• Catalog Number: AE22502
• Chemical Name: 3-Phenylcyclohex-2-en-1-one
• CAS Number: 10345-87-6
• Molecular Formula: C12H12O
• Molecular Weight: 172.2231
• MDL Number: MFCD00029515
• SMILES: O=C1CCCC(=C1)c1ccccc1
• NSC Number: 63067

Computed Properties

• Complexity: 221
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.1

Upstream Synthesis Route

5,6-Dihydro[1,1'-biphenyl]-3(4H)-one, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized for the construction of various organic molecules due to its unique structure and reactivity. In chemical synthesis, $name$ serves as a key intermediate in the preparation of biologically active compounds, pharmaceuticals, and advanced materials.One of the main applications of 5,6-Dihydro[1,1'-biphenyl]-3(4H)-one is in the synthesis of heterocyclic compounds. By functionalizing the biphenyl core, chemists can explore diverse synthetic pathways to access a range of fused ring systems with potential biological activities. Additionally, the presence of a ketone group in $name$ allows for further derivatization via various chemical reactions, enabling the introduction of different functional groups for fine-tuning the properties of the final products.Moreover, the unique structure of 5,6-Dihydro[1,1'-biphenyl]-3(4H)-one offers synthetic chemists opportunities for stereochemical control during transformations, leading to the production of chiral compounds with high enantioselectivity. This compound serves as a valuable starting material for the preparation of ligands, catalysts, and complex organic molecules with defined three-dimensional structures.Overall, the diverse applications of 5,6-Dihydro[1,1'-biphenyl]-3(4H)-one in chemical synthesis highlight its significance as a key building block for the creation of intricate organic compounds with potential applications in medicinal chemistry, materials science, and other fields of research.

Literature

• Synthesis and screening of small molecule inhibitors of anthrax edema factor.

  Bioorganic & medicinal chemistry letters 20080715

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501