591-55-9 | 5-Aminopyrimidine

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$15.00	$10.00
1g	>97%	in stock	$19.00	$13.00
5g	>97%	in stock	$63.00	$44.00
25g	98%	in stock	$226.00	$158.00

Description

• Catalog Number: AB45204
• Chemical Name: 5-Aminopyrimidine
• CAS Number: 591-55-9
• Molecular Formula: C4H5N3
• Molecular Weight: 95.1026
• MDL Number: MFCD01529870
• SMILES: Nc1cncnc1
• NSC Number: 401237

Computed Properties

• Complexity: 48.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: -0.7

Upstream Synthesis Route

As a professional chemist, I can tell you that 5-Aminopyrimidine is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Due to its unique molecular structure, 5-Aminopyrimidine can participate in a variety of reactions and transformations, making it a valuable intermediate in organic chemistry.In chemical synthesis, 5-Aminopyrimidine can be used to introduce the pyrimidine moiety into target molecules, facilitating the creation of new compounds with desired properties. Its amino group can undergo selective functionalization, allowing for the attachment of different functional groups to tailor the final product's characteristics. Additionally, 5-Aminopyrimidine can serve as a nitrogen-containing heterocyclic scaffold, imparting specific biological activities to the synthesized compounds.Overall, the application of 5-Aminopyrimidine in chemical synthesis is vital for the development of novel compounds with diverse functionalities and applications in various industries. Its versatility and reactivity make it a valuable tool for organic chemists seeking to create innovative molecules with specific properties.

Literature

• Compound instability in dimethyl sulphoxide, case studies with 5-aminopyrimidines and the implications for compound storage and screening.

  Bioorganic & medicinal chemistry letters 20121015

• Evaluation of electrophilic heteroaromatic substitution: synthesis of heteroaromatic-fused pyrimidine derivatives via sequential three-component heterocyclization.

  The Journal of organic chemistry 20121005

• 2-Amino-pyrimidinium picrate.

  Acta crystallographica. Section E, Structure reports online 20080101

• Biosynthesis of riboflavin: studies on the mechanism of GTP cyclohydrolase II.

  The Journal of biological chemistry 20010622