1124-63-6 | 3-Cyclohexyl-1-propanol

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$16.00	$11.00
1g	98%	in stock	$18.00	$12.00
5g	98%	in stock	$30.00	$21.00
25g	98%	in stock	$62.00	$44.00

Description

• Catalog Number: AB64848
• Chemical Name: 3-Cyclohexyl-1-propanol
• CAS Number: 1124-63-6
• Molecular Formula: C9H18O
• Molecular Weight: 142.23862
• MDL Number: MFCD00001528
• SMILES: OCCCC1CCCCC1
• NSC Number: 20787

Computed Properties

• Complexity: 74.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 3

Upstream Synthesis Route

3-Cyclohexylpropan-1-ol is a versatile compound commonly used in chemical synthesis for its valuable applications. This compound plays a key role in organic chemistry as a building block for the synthesis of various derivatives and functionalized molecules. Its primary function lies in its ability to serve as a precursor for the preparation of a wide range of compounds with diverse properties.In chemical synthesis, 3-Cyclohexylpropan-1-ol can undergo various reactions such as oxidation, reduction, esterification, and dehydration to yield different derivatives. For instance, it can be oxidized to form 3-Cyclohexylpropanal, a key intermediate in the synthesis of fragrances and pharmaceuticals. Furthermore, its ability to undergo esterification allows for the production of ester derivatives with unique properties for use in the fragrance and flavor industry.Additionally, 3-Cyclohexylpropan-1-ol can be used as a chiral building block in asymmetric synthesis, enabling the preparation of enantiomerically pure compounds. This compound's cyclohexyl group provides steric hindrance, which can influence the stereochemistry of the final product in a controlled manner.Overall, the versatility of 3-Cyclohexylpropan-1-ol in chemical synthesis makes it a valuable reagent for the creation of complex organic molecules with diverse applications in industries such as pharmaceuticals, fragrances, and materials science.

Literature

• SO3H-functionalized ionic liquid: efficient catalyst for bagasse liquefaction.

  Bioresource technology 20111101

• The role of alkoxy group on the A ring of isoflavones in the inhibition of interleukin-5.

  Archives of pharmacal research 20070801

• The role of the hydrophobic group on ring A of chalcones in the inhibition of interleukin-5.

  Archives of pharmacal research 20061101