38116-61-9 | 2-Hydroxy-6-methylnicotinic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$9.00	$7.00
5g	95%	in stock	$21.00	$15.00
10g	95%	in stock	$29.00	$20.00
25g	95%	in stock	$54.00	$38.00

Description

• Catalog Number: AB62342
• Chemical Name: 2-Hydroxy-6-methylnicotinic acid
• CAS Number: 38116-61-9
• Molecular Formula: C7H7NO3
• Molecular Weight: 153.1354
• MDL Number: MFCD00006272
• SMILES: Cc1ccc(c(n1)O)C(=O)O
• NSC Number: 10728

Computed Properties

• Complexity: 275
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 0.9

Upstream Synthesis Route

2-Hydroxy-6-methylpyridine-3-carboxylic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block for various organic reactions. This compound is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties.In chemical synthesis, $name$ serves as a valuable starting material for the preparation of pyridine derivatives through various synthetic routes. Its hydroxy and carboxylic acid functional groups allow for easy manipulation and functionalization, making it a highly useful precursor in the development of complex organic molecules.Furthermore, the presence of the methyl substituent at the 6-position of the pyridine ring provides additional stereochemical diversity, enabling the fine-tuning of molecular properties for specific applications. As a result, $name$ is utilized in the synthesis of bioactive compounds, dyes, and advanced materials where precise control over molecular structure is essential.Overall, the application of 2-Hydroxy-6-methylpyridine-3-carboxylic acid in chemical synthesis underscores its significance as a versatile building block with broad utility in the creation of diverse organic compounds.

Literature

• Virtual fragment screening for novel inhibitors of 6-phosphogluconate dehydrogenase.

  Bioorganic & medicinal chemistry 20100715