1006-23-1 | 2,4,6-Pyrimidinetriamine, 5-nitroso-

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$15.00	$11.00
25g	98%	in stock	$25.00	$18.00
100g	98%	in stock	$81.00	$57.00

Description

• Catalog Number: AA02975
• Chemical Name: 2,4,6-Pyrimidinetriamine, 5-nitroso-
• CAS Number: 1006-23-1
• Molecular Formula: C4H6N6O
• Molecular Weight: 154.13004
• MDL Number: MFCD00006096
• SMILES: O=Nc1c(N)nc(nc1N)N

Computed Properties

• Complexity: 140
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 7
• Hydrogen Bond Donor Count: 3
• XLogP3: -0.9

Upstream Synthesis Route

5-Nitroso-2,4,6-triaminopyrimidine, also known as $name$, is a versatile compound with significant applications in chemical synthesis. This compound plays a crucial role in organic reactions as a key reagent or intermediate, facilitating the creation of various complex molecules.1. Cross-Coupling Reactions: $name$ is commonly utilized in cross-coupling reactions, where it acts as a vital component in forming carbon-carbon or carbon-nitrogen bonds. These reactions are important in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.2. Nitrosation Reactions: Through nitrosation reactions, $name$ enables the introduction of nitroso functional groups into organic molecules. This functional group can serve as a precursor for further transformations, allowing for the synthesis of diverse compounds with valuable properties.3. Heterocyclic Synthesis: The unique structure of $name$ makes it a valuable building block in the construction of heterocyclic compounds. By incorporating this compound into synthetic pathways, chemists can access a wide range of heterocycles with varied applications in medicinal chemistry and materials science.4. Electrophilic Amination: $name$ can participate in electrophilic amination reactions, leading to the selective introduction of amino groups into target molecules. This reactivity is essential for the preparation of amino-substituted compounds that are pivotal in drug development and organic materials synthesis.5. Reductive Amination: In reductive amination processes, $name$ serves as a key reactant for the formation of secondary and tertiary amines. This transformation is crucial for the modification of functional groups in organic molecules, allowing for the creation of structurally diverse compounds.Overall, the applications of 5-Nitroso-2,4,6-triaminopyrimidine in chemical synthesis are diverse and pivotal for the creation of intricate organic compounds with varied functionalities. This compound acts as a valuable tool for synthetic chemists seeking to design and produce novel molecules with tailored properties and applications.