cas 92165-95-2|| where to buy (4-(Aziridin-1-yl)-2-((3,4-dichlorobenzyl)thio)pyrimidin-5-yl)methanol

Nom du produit:(4-(Aziridin-1-yl)-2-((3,4-dichlorobenzyl)thio)pyrimidin-5-yl)methanol

IUPAC Name:[4-(aziridin-1-yl)-2-{[(3,4-dichlorophenyl)methyl]sulfanyl}pyrimidin-5-yl]methanol

: CAS：92165-95-2; Formule moléculaire：C14H13Cl2N3OS; Pureté：95+%

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: N° CAS:92165-95-2; Formule moléculaire:C14H13Cl2N3OS; Point de fusion:-; Code SMILES:OCC1=CN=C(SCC2=CC=C(Cl)C(Cl)=C2)N=C1N3CC3; Densité:

: Numéro de catalogue:CM292777; Poids moléculaire:342.24; Point d'ébullition:; N° Mdl:; Stockage:

: Pyrimidines; Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.

: Aziridines; Aziridines are highly strained three-membered heterocyclic molecules composed of one amine group and two carbon units. They are aza analogs of epoxides. Aziridines are a very important class of synthetic building blocks and intermediates in organic synthesis, which are widely used in organic synthesis, especially in the synthesis of nitrogen-containing natural products. Due to the high ring tension of aziridine, its reactivity is high. Under certain conditions, it can undergo cycloaddition reaction with various dipolar reagents to prepare some new nitrogen-containing heterocyclic compounds.; Aziridines are a very important class of synthetic building blocks and intermediates in organic synthesis; Aziridines,; Aziridines are highly strained three-membered heterocyclic molecules composed of one amine group and two carbon units. They are aza analogs of epoxides.