118175-10-3 | 2-Hydroxymethyl-3-methyl-4-(3-methoxypropanoxyl)pyridine

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$14.00	$10.00
1g	98%	in stock	$20.00	$14.00
5g	98%	in stock	$49.00	$34.00
25g	98%	in stock	$142.00	$100.00
100g	98%	in stock	$473.00	$331.00

Description

• Catalog Number: AE11676
• Chemical Name: 2-Hydroxymethyl-3-methyl-4-(3-methoxypropanoxyl)pyridine
• CAS Number: 118175-10-3
• Molecular Formula: C11H17NO3
• Molecular Weight: 211.25757999999993
• MDL Number: MFCD08274729
• SMILES: Cc1c(OCCCOC)ccnc1CO

Computed Properties

• Complexity: 166
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• XLogP3: 0.5

Upstream Synthesis Route

The compound (4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methanol is a versatile building block in chemical synthesis, commonly utilized for its unique structural features and functional groups. With its substituted pyridine ring and alcohol moiety, this compound serves as a valuable intermediate in the preparation of diverse organic compounds.In chemical synthesis, (4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methanol can participate in various reactions to introduce additional functional groups or modify its existing structure. Its alcohol group can undergo reactions such as esterification, oxidation, or substitution, providing opportunities for further derivatization. Additionally, the substituted pyridine ring offers a platform for the introduction of different substituents, enabling the synthesis of specialized molecules for various applications.This compound can be employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its ability to serve as a scaffold for molecular modifications. Its inclusion in synthetic pathways can lead to the creation of compounds with enhanced biological activities, improved chemical properties, or specific functionalities tailored to the desired application. Furthermore, the presence of both aromatic and aliphatic functionalities in (4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methanol imparts flexibility in its reactivity and opens up possibilities for diverse chemical transformations.Overall, (4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methanol plays a crucial role in chemical synthesis by offering a strategic starting point for the construction of complex organic molecules with targeted properties and applications. Its structural versatility and reactivity make it a valuable component in the synthesis of a wide range of valuable compounds across various industries.

Literature

• Structural elucidation of rabeprazole sodium photodegradation products.

  Journal of pharmaceutical and biomedical analysis 20080107