502-41-0 | Cycloheptanol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$48.00	$33.00
100g	98%	in stock	$163.00	$114.00
500g	98%	in stock	$750.00	$525.00

Description

• Catalog Number: AB45794
• Chemical Name: Cycloheptanol
• CAS Number: 502-41-0
• Molecular Formula: C7H14O
• Molecular Weight: 114.1855
• MDL Number: MFCD00004150
• SMILES: OC1CCCCCC1
• NSC Number: 52221

Computed Properties

• Complexity: 53.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• XLogP3: 1

Upstream Synthesis Route

Cycloheptanol is a versatile compound that finds wide application in chemical synthesis due to its unique structure and reactivity. In organic chemistry, it serves as a key intermediate in the preparation of various important compounds. By undergoing various chemical reactions, Cycloheptanol can be transformed into different functional groups, making it an essential building block for the synthesis of pharmaceuticals, fragrances, and other complex organic molecules. Its hydroxyl group can undergo esterification, oxidation, or reduction reactions to yield a wide range of derivatives with diverse properties and functionalities. Additionally, the cyclic nature of Cycloheptanol imparts specific stereochemical characteristics to the products formed, making it valuable in the design and synthesis of chiral molecules. The ability of Cycloheptanol to participate in multiple types of reactions makes it a versatile tool for organic chemists in the creation of new compounds with tailored properties and applications.

Literature

• Disentangling the secondary relaxations in the orientationally disordered mixed crystals: cycloheptanol + cyclooctanol two-component system.

  The journal of physical chemistry. B 20100513

• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-induced cyclizations.

  Beilstein journal of organic chemistry 20100101

• Study of supercooled orientationally disordered binary solid solutions II: cyclohexyl derivatives, neopentanol and neopentylglycol.

  Physical chemistry chemical physics : PCCP 20091028

• Dielectric and calorimetric study of orientationally disordered phases in two unusual two-component systems.

  The journal of physical chemistry. B 20080306

• Fluorescent detection for cyclic and acyclic alcohol guests by naphthalene-appended amino-beta-cyclodextrins.

  Organic letters 20061026

• Thermodynamics of the molecular and chiral recognition of cycloalkanols and camphor by modified beta-cyclodextrins possessing simple aromatic tethers.

  The Journal of organic chemistry 20040109

• [Lipase-catalyzed kinetic resolution of 2-substituted cycloalkanols].

  Acta pharmaceutica Hungarica 20010101