Nom du produit:2-((Methylamino)methyl)thieno[3,2-d]pyrimidin-4(3H)-one hydrochloride

IUPAC Name:2-[(methylamino)methyl]-3H,4H-thieno[3,2-d]pyrimidin-4-one hydrochloride

CAS:923216-51-7
Formule moléculaire:C8H10ClN3OS
Pureté:95%
Numéro de catalogue:CM151517
Poids moléculaire:231.7

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CM151517-1g in stock ǟǟij

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Détails du produit

N° CAS:923216-51-7
Formule moléculaire:C8H10ClN3OS
Point de fusion:-
Code SMILES:O=C1C2=C(C=CS2)N=C(CNC)N1.[H]Cl
Densité:
Numéro de catalogue:CM151517
Poids moléculaire:231.7
Point d'ébullition:
N° Mdl:
Stockage:Store at room temperature.

Category Infos

Thienopyrimidines
Thienopyrimidines are a class of heterocyclic compounds with diverse biological activities depending on their detailed substitution patterns. In addition, many thienopyrimidine derivatives have shown potent activity against cancer cell lines and specific oncogenes.

Column Infos

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Product Other Information

Product Overview 2-((Methylamino)methyl)thieno[3,2-d]pyrimidin-4(3H)-one hydrochloride (also known as 4-Methyl-3-thienyl-2-pyrimidinamine hydrochloride, or 4-Methylamino-3-thienyl-2-pyrimidinamine hydrochloride) is a synthetic compound with potential applications in the field of medicinal chemistry. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound.
Synthesis Method 2-((Methylamino)methyl)thieno[3,2-d]pyrimidin-4(3H)-one hydrochloride can be synthesized using a variety of methods. One method involves the condensation of 4-methylthiophenol with anhydrous hydrazine hydrate in the presence of an acid catalyst, such as hydrochloric acid or acetic acid. The resulting product is then purified by recrystallization from ethanol or ethyl acetate.
Chemical Properties It is a relatively stable compound, and can be easily synthesized using a variety of methods. It is also relatively inexpensive, and can be obtained from a variety of sources. It is not a particularly soluble compound, and can be difficult to work with in certain laboratory applications.
Synthesis and Application It has been used as a starting material for the synthesis of a variety of compounds with potential therapeutic applications. It has been used in the synthesis of compounds that show potential activity against the human immunodeficiency virus (HIV), as well as compounds that show potential activity against the herpes simplex virus (HSV). It has also been used in the synthesis of compounds that show potential activity against the human papillomavirus (HPV).
Future Directions Potential future directions include further research into its potential anti-viral, anti-cancer, anti-inflammatory, and anti-oxidant properties. Additionally, further research into its potential applications in the field of medicinal chemistry, including the synthesis of compounds with potential therapeutic applications, is warranted. Finally, further research into its potential uses in the development of novel drug delivery systems is also of interest.