16681-71-3 | 1-Methyl-1h-1,2,3-triazole-4-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$155.00	$108.00
250mg	95%	in stock	$219.00	$153.00
1g	95%	in stock	$533.00	$373.00
5g	95%	in stock	$2,314.00	$1,620.00

Description

• Catalog Number: AD68532
• Chemical Name: 1-Methyl-1h-1,2,3-triazole-4-carboxylic acid
• CAS Number: 16681-71-3
• Molecular Formula: C4H5N3O2
• Molecular Weight: 127.1014
• MDL Number: MFCD08689473
• SMILES: Cn1cc(nn1)C(=O)O

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: -0.5

Upstream Synthesis Route

1-Methyl-1H-1,2,3-triazole-4-carboxylic acid is a versatile compound commonly utilized in chemical synthesis for its unique reactivity and structural properties. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 1-Methyl-1H-1,2,3-triazole-4-carboxylic acid can act as a key intermediate in the preparation of heterocyclic compounds, which are essential in drug discovery and development. Its triazole ring structure offers opportunities for functionalization and diversification, allowing for the creation of new molecules with potential biological activities.Furthermore, the carboxylic acid group present in this compound enables it to participate in a wide range of chemical reactions, such as amide bond formation, esterification, and metal-catalyzed transformations. This reactivity makes 1-Methyl-1H-1,2,3-triazole-4-carboxylic acid a valuable tool for building complex molecular architectures in organic synthesis.Overall, the application of 1-Methyl-1H-1,2,3-triazole-4-carboxylic acid in chemical synthesis showcases its significance in advancing research and development across various industries, highlighting its role as a key component in the creation of novel compounds with diverse functionalities.

Literature

• Inhibitor scaffold for the histone lysine demethylase KDM4C (JMJD2C).

  Bioorganic & medicinal chemistry letters 20120915