823-76-7 | Cyclohexyl methyl ketone

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$8.00	$6.00
5g	97%	in stock	$27.00	$19.00
10g	97%	in stock	$38.00	$27.00
25g	97%	in stock	$75.00	$53.00
50g	97%	in stock	$150.00	$105.00
100g	97%	in stock	$277.00	$194.00

Description

• Catalog Number: AB43333
• Chemical Name: Cyclohexyl methyl ketone
• CAS Number: 823-76-7
• Molecular Formula: C8H14O
• Molecular Weight: 126.1962
• MDL Number: MFCD00040418
• SMILES: CC(=O)C1CCCCC1
• NSC Number: 16249

Computed Properties

• Complexity: 101
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2

Upstream Synthesis Route

1-Cyclohexylethan-1-one, also known as cyclohexyl ethyl ketone, is a valuable compound widely utilized in chemical synthesis for various applications. One of its primary uses is as a building block in the preparation of pharmaceuticals and agrochemicals. Due to its unique structure and reactivity, 1-Cyclohexylethan-1-one serves as a versatile intermediate in the synthesis of complex organic molecules. Additionally, this compound can be employed in the production of fragrances and flavoring agents due to its characteristic odor profile. In organic chemistry, 1-Cyclohexylethan-1-one is often utilized as a starting material for the synthesis of numerous functional groups, making it an essential component in the creation of diverse chemical compounds. Furthermore, its compatibility with various reaction conditions and ease of manipulation in synthetic processes make it a valuable tool for researchers and chemists seeking to develop novel molecules with specific properties.

Literature

• The role of acid catalysis in the Baeyer-Villiger reaction. A theoretical study.

  The Journal of organic chemistry 20120817

• Cloning, expression and characterization of a eukaryotic cycloalkanone monooxygenase from Cylindrocarpon radicicola ATCC 11011.

  Applied microbiology and biotechnology 20120501

• Simple in situ monitoring of a complex catalytic reaction network at high pressure by attenuated total reflection Fourier transform infrared spectroscopy.

  Applied spectroscopy 20100301

• Computational study of the factors controlling enantioselectivity in ruthenium(II) hydrogenation catalysts.

  Inorganic chemistry 20080407