10030-78-1 | 2-(Methylamino)-6,7-dihydro-3h-purin-6-one

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$78.00	$54.00
250mg	95%	in stock	$99.00	$69.00
1g	95%	in stock	$227.00	$159.00

Description

• Catalog Number: AA01781
• Chemical Name: 2-(Methylamino)-6,7-dihydro-3h-purin-6-one
• CAS Number: 10030-78-1
• Molecular Formula: C6H7N5O
• Molecular Weight: 165.1527
• MDL Number: MFCD00127896
• SMILES: CNc1[nH]c(=O)c2c(n1)[nH]cn2

Upstream Synthesis Route

The compound $name$ is a versatile building block commonly utilized in chemical synthesis due to its unique properties and reactivity. In the realm of organic chemistry, it serves as a key intermediate for the preparation of various biologically active compounds and pharmaceutical agents. Its structural framework contains essential functional groups that enable facile transformations, making it a valuable tool for synthesizing complex molecules.One of the crucial applications of 6H-Purin-6-one,1,9-dihydro-2-(methylamino)- in chemical synthesis is its role as a precursor for the synthesis of nucleoside analogs. By strategically modifying the methylamino group or functionalizing the purine ring, chemists can access a diverse array of nucleoside derivatives with potential therapeutic applications. Furthermore, this compound can be employed in the construction of nucleotide analogs and nucleic acid mimics, offering a platform for exploring structure-activity relationships in drug design and discovery.Additionally, the reactivity of 6H-Purin-6-one,1,9-dihydro-2-(methylamino)- lends itself to the formation of heterocyclic compounds and fused ring systems. Through cyclization reactions and cross-coupling methodologies, chemists can harness the structural diversity of this compound to access a wide range of heterocycles with varying substitution patterns and functionalities. This versatility makes it a valuable building block for designing novel molecular scaffolds and investigating new chemical transformations.Overall, the utility of 6H-Purin-6-one,1,9-dihydro-2-(methylamino)- in chemical synthesis extends beyond its individual structure, offering a gateway to the synthesis of diverse organic compounds with potential biological activities and pharmacological properties. Its role as a synthetic precursor underscores its significance in modern organic chemistry and drug development efforts.