Pyrimido[4,5-d]pyrimidin-4-amine is a heterocyclic organic compound characterized by its fused pyrimidine rings, which contribute to its unique chemical properties. This compound features an amino group at the 4-position of the pyrimidine ring, enhancing its potential for various chemical reactions and biological activities. It is typically a crystalline solid at room temperature and may exhibit solubility in polar solvents, depending on the specific conditions. The presence of nitrogen atoms in its structure can influence its reactivity, making it a candidate for applications in medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, its structural characteristics may allow for interactions with biological targets, which is of interest in drug design. The compound's CAS number, 26979-05-5, serves as a unique identifier in chemical databases, facilitating research and information retrieval. Overall, pyrimido[4,5-d]pyrimidin-4-amine is notable for its structural complexity and potential utility in various chemical and biological applications.

pyrimido[4,5-d]pyrimidin-4-amine

26979-05-5: 26979-05-5, Pyrimido[4,5-d]pyrimidin-4-ylamine,  Pyrimido[4,5-d]pyrimidin-4-amine

Pyrimido[4,5-d]pyrimidin-4-amine

Pyrimido[4,5-d]pyrimidin-4-amine is an isothiocyanate with a potential use in combinatorial chemistry. It is a reagent for the synthesis of pyrimidines and purines. Pyrimido[4,5-d]pyrimidin-4-amine can be synthesized by reacting phenyl isothiocyanate with thiourea. This compound has been shown to react with various nucleophiles at the methylene group to form amides or ureas. 
Pyrimido[4,5-d]pyrimidin-4-amine has also been shown to be useful as a spectroscopic probe for studying the mechanisms of nucleophilic substitution reactions.

CAS 26979-05-5: pyrimido[4,5-d]pyrimidin-4-amine

Pyrimido[4,5-d]pyrimidin-4-amine

Ref: 10-F321501

Pyrimido[4,5-d]pyrimidin-4-amine

Ref: 3D-BBA97905

Pyrimido[4,5-d]pyrimidin-4-amine

Ref: IN-DA003KS3