CAS 18588-49-3
:5-Phenyl-2,4-pyrimidinediamine
Description:
5-Phenyl-2,4-pyrimidinediamine, with the CAS number 18588-49-3, is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at the 2 and 4 positions. This compound features a phenyl group attached to the 5-position of the pyrimidine ring, contributing to its aromatic properties. It is a diamine, indicating the presence of two amino groups (-NH2) at the 2 and 4 positions of the pyrimidine, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of these functional groups makes it potentially useful in the synthesis of pharmaceuticals, agrochemicals, and dyes. Additionally, the compound may exhibit biological activity, although specific biological properties would depend on further studies. Its solubility, stability, and reactivity can vary based on environmental conditions such as pH and temperature. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C10H10N4
InChI:InChI=1S/C10H10N4/c11-9-8(6-13-10(12)14-9)7-4-2-1-3-5-7/h1-6H,(H4,11,12,13,14)
InChI key:InChIKey=FUVWRUJASRBHEK-UHFFFAOYSA-N
SMILES:NC=1C(C2=CC=CC=C2)=CN=C(N)N1
Synonyms:- 2,4-Diamino-5-phenylpyrimidine
- 2,4-Pyrimidinediamine, 5-Phenyl-
- Pyrimidine, 2,4-diamino-5-phenyl-
- 5-Phenyl-2,4-pyrimidinediamine
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Found 2 products.
5-Phenylpyrimidine-2,4-diamine
CAS:<p>5-Phenylpyrimidine-2,4-diamine is an antiparasitic agent that belongs to the group of derivs. It has been shown to inhibit coccidian growth in vitro and has antiparasitic activity against bacteria and protozoa. 5-Phenylpyrimidine-2,4-diamine binds to the enzyme acetyl coenzyme A synthetase in the parasite's mitochondria and prevents the synthesis of ATP. This leads to cell death.</p>Formula:C10H10N4Purity:Min. 95%Molecular weight:186.21 g/mol
