1004-39-3 | 4,6-Diamino-2-mercaptopyrimidine

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$7.00	$5.00
10g	97%	in stock	$20.00	$14.00
25g	97%	in stock	$48.00	$34.00
100g	97%	in stock	$184.00	$129.00
500g	97%	in stock	$839.00	$587.00

Description

• Catalog Number: AA02281
• Chemical Name: 4,6-Diamino-2-mercaptopyrimidine
• CAS Number: 1004-39-3
• Molecular Formula: C4H6N4S
• Molecular Weight: 142.1822
• MDL Number: MFCD00149406
• SMILES: Nc1cc(N)[nH]c(=S)n1

Computed Properties

• Complexity: 205
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 3
• XLogP3: -1.2

Upstream Synthesis Route

The versatile compound 4,6-Diaminopyrimidine-2-thiol, also known as DAPT, is a valuable building block in chemical synthesis. This heterocyclic compound plays a crucial role in the preparation of various organic molecules and pharmaceuticals. In chemical synthesis, 4,6-Diaminopyrimidine-2-thiol is commonly used as a key intermediate in the production of dyes, drugs, and agrochemicals. Its unique structure and reactivity allow for the formation of complex molecular structures with specific properties. Additionally, this compound serves as a precursor for the synthesis of biologically active compounds, including anticancer and antiviral drugs.Due to its ability to participate in diverse chemical reactions, 4,6-Diaminopyrimidine-2-thiol is employed in the creation of new materials with tailored properties. Its role in the synthesis of polymeric materials, such as conducting polymers and gels, highlights its significance in material science. Furthermore, the incorporation of this compound in the development of sensors and catalysts demonstrates its wide-ranging applications in various fields of chemistry.Overall, 4,6-Diaminopyrimidine-2-thiol is a versatile compound that contributes significantly to chemical synthesis by enabling the construction of complex organic molecules and materials with diverse functionalities.

Literature

• 4,6-Diaminopyrimidine-2(1H)-thione hemihydrate: a three-dimensional hydrogen-bonded framework.

  Acta crystallographica. Section C, Crystal structure communications 20121001

• Determination of ammonium ion using a reagentless amperometric biosensor based on immobilized alanine dehydrogenase.

  Sensors (Basel, Switzerland) 20110101

• Raman characterization of monolayers formed from mixtures of sodium 2-mercaptoethanesulfonate and various aromatic mercapto-derivative bases.

  The journal of physical chemistry. B 20100422

• Bis(4,6-diamino-pyrimidin-2-yl) disulfide dimethyl sufoxide disolvate.

  Acta crystallographica. Section E, Structure reports online 20080901

• Synthesis, Spectroscopic, and Anticancerous Properties of Mixed Ligand Palladium(II) and Silver(I) Complexes with 4,6-Diamino-5-hydroxy-2-mercaptopyrimidine and 2,2'-Bipyridyl.

  Metal-based drugs 20080101

• Mediatorless voltammetric oxidation of NADH and sensing of ethanol.

  Biosensors & bioelectronics 20051215