13482-22-9 | 4-Hydroxycyclohexanone

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$5.00	$4.00
1g	98%	in stock	$8.00	$6.00
5g	98%	in stock	$23.00	$17.00
10g	98%	in stock	$45.00	$32.00
25g	98%	in stock	$100.00	$70.00
50g	98%	in stock	$200.00	$140.00

Description

• Catalog Number: AB45033
• Chemical Name: 4-Hydroxycyclohexanone
• CAS Number: 13482-22-9
• Molecular Formula: C6H10O2
• Molecular Weight: 114.1424
• MDL Number: MFCD02093817
• SMILES: OC1CCC(=O)CC1

Computed Properties

• Complexity: 88.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: -0.2

Upstream Synthesis Route

4-Hydroxycyclohexanone is a versatile compound utilized in various chemical synthesis processes. Its primary application lies in the field of organic chemistry, where it serves as a key intermediate for synthesizing a wide range of complex organic compounds. This compound is particularly valued for its role in the production of pharmaceuticals, agrochemicals, and fragrance ingredients. In organic synthesis, 4-Hydroxycyclohexanone can undergo various reactions such as oxidation, reduction, and functional group transformations to yield structurally diverse molecules with valuable properties. Its hydroxyl group and cyclohexanone framework make it a valuable building block for creating new chemical entities with potential applications in medicinal chemistry, materials science, and other related disciplines. The unique reactivity and structural features of 4-Hydroxycyclohexanone make it an indispensable component in the toolbox of synthetic chemists aiming to design and develop novel, biologically active compounds and functional materials.

Literature

• The thio-adduct facilitated, enzymatic kinetic resolution of 4-hydroxycyclopentenone and 4-hydroxycyclohexenone.

  Organic & biomolecular chemistry 20100207

• New bioorganic reagents: evolved cyclohexanone monooxygenase--why is it more selective?

  The Journal of organic chemistry 20061027

• Microbial Baeyer-Villiger oxidation: stereopreference and substrate acceptance of cyclohexanone monooxygenase mutants prepared by directed evolution.

  Organic letters 20060316