
CAS 51391-96-9
:5-Methylcyclocytidine hydrochlorine
Description:
5-Methylcyclocytidine hydrochloride is a modified nucleoside that is part of the broader category of nucleoside analogs. It features a cyclopentane ring fused to a pyrimidine base, which contributes to its unique structural properties. This compound is characterized by the presence of a methyl group at the 5-position of the cytidine base, which can influence its biological activity and stability. As a hydrochloride salt, it is typically more soluble in water, facilitating its use in various biochemical applications. 5-Methylcyclocytidine has garnered interest in research, particularly in the fields of molecular biology and medicinal chemistry, due to its potential role in RNA modification and its implications in therapeutic development. Its properties, such as melting point, solubility, and reactivity, can vary based on the specific conditions and formulations used. Overall, this compound represents a significant area of study for understanding nucleoside function and the development of antiviral and anticancer agents.
- CMC.HCl
- Cmc・Hci
- (2R-(2Alpha,3Beta,3Abeta,9Abeta))-2,3,3A,9A-Tetrahydro-3-Hydroxy-6-Imino-7-Methyl-6H-Furo(2',3':4,5)Oxazolo(3,2-A)Pyrimidine-2-Methanol Monohydrochloride
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Found 5 products.
5-Methylcyclocytidine hydrochloride
CAS:5-Methylcyclocytidine hydrochloridePurity:95%Molecular weight:275.69g/molO-2,3'-Anhydro-5-methylcytidine hydrochloride
CAS:O-2,3'-Anhydro-5-methylcytidine hydrochloride is a Nucleoside Derivative - 3'-Modified nucleoside.Formula:C10H14ClN3O4Color and Shape:SolidMolecular weight:275.695-Methylcyclocytidine hydrochlorine
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:275.695-Methylcyclocytidine Hydrochlorine
CAS:Controlled Product<p>Applications 5-Methylcyclocytidine Hydrochlorine is an intermediate in the synthesis of 1-β-D-Arabinofuranosyl-5-methylcytosine (A774180) which is a potential antiviral nucleoside.<br>References Birnbaum, G. I., et al.: J. Am. Chem. Soc., 105, 5398 (1983), Gentry, G. A., et al.: Antiviral Chemother.: Des. Inhib. Viral Funct., [Proc. Symp. Antiviral Chemother.], 61, (1981)<br></p>Formula:C10H13N3O4·HClColor and Shape:NeatMolecular weight:275.69




