100516-88-9 | 6-Quinolinylmethanol

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$18.00	$13.00
1g	97%	in stock	$36.00	$25.00
5g	97%	in stock	$115.00	$81.00
25g	97%	in stock	$199.00	$139.00

Description

• Catalog Number: AA02700
• Chemical Name: 6-Quinolinylmethanol
• CAS Number: 100516-88-9
• Molecular Formula: C10H9NO
• Molecular Weight: 159.18456
• MDL Number: MFCD03789621
• SMILES: OCc1ccc2c(c1)cccn2

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.3

Upstream Synthesis Route

Quinolin-6-ylmethanol is a versatile organic compound widely used in chemical synthesis. Its primary application lies in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure, Quinolin-6-ylmethanol serves as a valuable building block in the synthesis of complex molecules.In pharmaceutical synthesis, Quinolin-6-ylmethanol is utilized as a key intermediate in the preparation of diverse biologically active compounds. Its presence in drug development allows for the modification of specific properties, such as solubility, potency, and bioavailability. This flexibility makes it a crucial component in the creation of novel therapeutic agents.Additionally, Quinolin-6-ylmethanol plays a significant role in agrochemical research and development. Its incorporation into pesticide formulations, herbicides, and fungicides enhances the efficiency and selectivity of agricultural products. By utilizing Quinolin-6-ylmethanol in the synthesis of agrochemicals, researchers can address pest resistance, environmental concerns, and plant health with improved precision.Furthermore, in the realm of specialty chemicals, Quinolin-6-ylmethanol contributes to the synthesis of various compounds used in diverse industrial applications. Its structural attributes enable chemists to design customized molecules for specific functions, including materials science, catalysis, and polymer chemistry. By leveraging the versatility of Quinolin-6-ylmethanol, scientists can develop innovative solutions for a wide range of industrial challenges.

Literature

• Design, synthesis and pharmacological evaluation of 6-hydroxy-4-methylquinolin-2(1H)-one derivatives as inotropic agents.

  Journal of enzyme inhibition and medicinal chemistry 20090801

• Inotropic and chronotropic effects of 6-hydroxy-4-methylquinolin-2(1H)-one derivatives in isolated rat atria.

  Iranian biomedical journal 20080401