1027338-06-2 | 3-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$220.00	$154.00
250mg	95%	in stock	$396.00	$277.00
1g	95%	in stock	$1,178.00	$824.00

Description

• Catalog Number: AA10487
• Chemical Name: 3-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne
• CAS Number: 1027338-06-2
• Molecular Formula: C16H12O
• Molecular Weight: 220.2659
• MDL Number: MFCD10699137
• SMILES: OC1Cc2ccccc2C#Cc2c1cccc2

Computed Properties

• Complexity: 334
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 3.1

Upstream Synthesis Route

5-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne is a versatile compound that finds widespread application in chemical synthesis. This molecule's unique structure and reactivity make it a valuable building block in organic chemistry. When used in synthesis, 5-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne serves as a key intermediate for the creation of various complex organic compounds.One significant application of 5-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne is in the formation of heterocyclic compounds. By utilizing its hydroxy and benzene rings, chemists can introduce functional groups and modify the structure of the molecule, leading to the synthesis of diverse heterocycles with unique properties and applications.Moreover, 5-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne can participate in Diels-Alder reactions, enabling the construction of polycyclic frameworks. The reaction of this compound with dienophiles under specific conditions allows for the regio- and stereoselective formation of fused ring systems, making it a valuable tool for the efficient synthesis of complex organic molecules.Additionally, the presence of a hydroxy group in 5-Hydroxy-1,2:5,6-dibenzocyclooct-7-yne provides opportunities for further functionalization through various chemical transformations. This hydroxyl functionality can undergo reactions such as esterification, etherification, or oxidation, expanding the molecule's synthetic versatility and enabling the preparation of a wide range of advanced intermediates and final products in chemical synthesis.