102074-19-1 | (5-Methylpyridin-3-yl)methanol

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$16.00	$11.00
1g	95%	in stock	$26.00	$18.00
5g	95%	in stock	$55.00	$39.00
10g	95%	in stock	$104.00	$73.00
25g	95%	in stock	$209.00	$147.00

Description

• Catalog Number: AA08338
• Chemical Name: (5-Methylpyridin-3-yl)methanol
• CAS Number: 102074-19-1
• Molecular Formula: C7H9NO
• Molecular Weight: 123.15246
• MDL Number: MFCD08236816
• SMILES: Cc1cc(CO)cnc1

Computed Properties

• Complexity: 85
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.3

Upstream Synthesis Route

The application of (5-Methylpyridin-3-yl)methanol in chemical synthesis lies in its versatile reactivity and unique properties. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and materials. Due to the presence of both a pyridine ring and a hydroxyl group, (5-Methylpyridin-3-yl)methanol can participate in a range of synthetic transformations, including oxidation, reduction, esterification, and substitution reactions.In organic synthesis, (5-Methylpyridin-3-yl)methanol can be used as a starting material to introduce functional groups at specific positions on the pyridine ring, allowing for the preparation of structurally diverse compounds. Furthermore, the hydroxyl group in this molecule can undergo various chemical modifications, enabling the attachment of other molecular fragments or the formation of esters, ethers, or amides.Additionally, (5-Methylpyridin-3-yl)methanol can act as a chelating ligand, coordinating with metal ions in catalytic processes or facilitating complexation reactions in coordination chemistry. Its presence can influence the stereochemistry and regioselectivity of certain reactions, leading to the formation of specific stereoisomers or positional isomers.Overall, the strategic incorporation of (5-Methylpyridin-3-yl)methanol into synthetic routes allows chemists to access novel chemical structures, enhance the efficiency of complex molecule assembly, and tailor the properties of final products for desired applications.