199296-51-0 | 4-(Aminomethyl)pyridin-2-amine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$68.00	$47.00
250mg	95%	in stock	$71.00	$50.00
1g	95%	in stock	$128.00	$89.00
5g	95%	in stock	$424.00	$297.00
25g	95%	in stock	$1,723.00	$1,206.00

Description

• Catalog Number: AB08684
• Chemical Name: 4-(Aminomethyl)pyridin-2-amine
• CAS Number: 199296-51-0
• Molecular Formula: C6H9N3
• Molecular Weight: 123.1558
• MDL Number: MFCD06213870
• SMILES: NCc1ccnc(c1)N

Computed Properties

• Complexity: 84.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: -0.9

Upstream Synthesis Route

4-(Aminomethyl)pyridin-2-amine, also known by its chemical formula C7H10N3, plays a crucial role in chemical synthesis as a versatile building block. With its unique structure combining aminomethyl and pyridine moieties, this compound serves as a valuable intermediate in the synthesis of various organic molecules. In chemical synthesis, 4-(Aminomethyl)pyridin-2-amine acts as a key precursor for the construction of complex organic compounds through different reaction pathways. Its amino group allows for selective functionalization reactions, enabling the attachment of various functional groups or modifications to its structure. This compound can undergo substitution reactions, condensation reactions, and other transformations to introduce new chemical entities to the molecule.The presence of the pyridine ring in 4-(Aminomethyl)pyridin-2-amine offers unique reactivity patterns, making it a versatile starting material in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its structural features make it an essential component in the development of biologically active compounds, coordination complexes, and organic dyes. This compound's utility in chemical synthesis extends to the creation of ligands, catalysts, and intermediates that are essential in modern organic chemistry research.Overall, 4-(Aminomethyl)pyridin-2-amine's strategic placement of functional groups and its reactivity make it a valuable asset in chemical synthesis, contributing to the creation of diverse and functionally rich organic molecules.