CAS 3546-50-7

2,5,6-Triaminopyrimidine

Description:

2,5,6-Triaminopyrimidine is an organic compound characterized by its pyrimidine ring structure, which contains three amino groups (-NH2) at the 2, 5, and 6 positions. This compound is a white to off-white crystalline solid that is soluble in water and polar organic solvents, reflecting its ability to form hydrogen bonds due to the presence of multiple amino groups. It exhibits basic properties, making it a potential candidate for various chemical reactions, including those involving nucleophilic substitution. 2,5,6-Triaminopyrimidine is of interest in medicinal chemistry and agricultural applications, particularly as a building block for the synthesis of pharmaceuticals and agrochemicals. Its structural features allow it to participate in biological processes, potentially influencing enzyme activity or acting as a precursor for more complex molecules. Safety data indicates that, like many amines, it should be handled with care due to potential irritant properties. Overall, 2,5,6-Triaminopyrimidine is a versatile compound with significant implications in both research and industrial applications.

Formula: C₄H₇N₅

InChI: InChI=1S/C4H7N5/c5-2-1-8-4(7)9-3(2)6/h1H,5H2,(H4,6,7,8,9)

InChI key: InChIKey=CSNFMBGHUOSBFU-UHFFFAOYSA-N

SMILES: NC=1C(N)=CN=C(N)N1

Synonyms:

• 2,4,5-Pyrimidinetriamine
• 2,4,5-Triaminopyrimidine
• 2,5,6-Triaminopyrimidine
• NSC 65987
• Pyrimidine, 2,4,5-triamino-

Pyrimidine-2,4,5-triamine

CAS: 3546-50-7

Formula: C₄H₇N₅

Color and Shape: Solid

Molecular weight: 125.1319

Ref: IN-DA00I71F

pyrimidine-2,4,5-triamine

CAS: 3546-50-7

Pyrimidine-2,4,5-triamine is a nucleotide derivative that is used to study the effects of extracellular Ca2+ on cell growth. It has anticancer activity and is used in the treatment of human immunodeficiency virus (HIV) infection and other inflammatory diseases. Pyrimidine-2,4,5-triamine has been shown to inhibit phosphatases, including malonic acid phosphatase and nitro phosphatase. This inhibition leads to an accumulation of malonic acid and nitro compounds which are cytotoxic. The drug also inhibits the production of hydrogen peroxide by inhibiting surface methodology enzymes such as peroxidase or catalase. Pyrimidine-2,4,5-triamine has been shown to be resistant to hydrolysis by hydrophobic effect enzymes such as esterases or glucuronidases. The drug also causes irreversible inhibition of DNA gyrase and topoisomerase

Formula: C₄H₇N₅

Purity: Min. 95%

Molecular weight: 125.13 g/mol

Ref: 3D-DAA54650