116-02-9 | 3,3,5-Trimethylcyclohexanol

Packsize	Purity	Availability	Price	Discounted Price
5g	80%	in stock	$19.00	$13.00
25g	80%	in stock	$42.00	$30.00
100g	80%	in stock	$125.00	$88.00
400g	80%	in stock	$259.00	$181.00

Description

• Catalog Number: AA22397
• Chemical Name: 3,3,5-Trimethylcyclohexanol
• CAS Number: 116-02-9
• Molecular Formula: C9H18O
• Molecular Weight: 142.2386
• MDL Number: MFCD00019378
• SMILES: CC1CC(O)CC(C1)(C)C
• NSC Number: 4008

Computed Properties

• Complexity: 118
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Undefined Atom Stereocenter Count: 2
• XLogP3: 2.6

Upstream Synthesis Route

3,3,5-Trimethylcyclohexanol, a versatile compound commonly used in chemical synthesis, serves as an essential building block for numerous industrial processes. Its unique structure and properties make it an ideal candidate for various applications in the synthesis of specialty chemicals, pharmaceuticals, and agricultural products.In chemical synthesis, 3,3,5-Trimethylcyclohexanol plays a crucial role as a key intermediate in the production of fragrances, flavors, and fine chemicals. Its compact and rigid molecular structure allows for precise control over stereochemistry during reactions, facilitating the synthesis of chiral compounds and complex molecules. Additionally, its high reactivity and functional group compatibility make it a valuable reagent for constructing carbon-carbon and carbon-heteroatom bonds, enabling the efficient assembly of intricate organic frameworks.Moreover, 3,3,5-Trimethylcyclohexanol exhibits excellent solubility in both organic solvents and water, enhancing its versatility in various synthetic transformations. Its stability under a wide range of experimental conditions further expands its utility in chemical research and development, making it a preferred choice for chemists and industrial manufacturers alike seeking to achieve synthetic efficiency and product quality.

Literature

• Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis.

  Journal of analytical methods in chemistry 20120101

• New attractants for males of the solanaceous fruit fly Bactrocera latifrons.

  Journal of chemical ecology 20081201