5417-83-4

Basic information

• Product Name: 1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one
• CAS NO: 5417-83-4
• Molecular Formula: C₇H₈N₄OS
• Molecular Weight: 196.2296
• Mol File: 5417-83-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 333.3°C at 760 mmHg
• Flash Point: 155.4°C
• Density: 1.59g/cm³
• Vapor Pressure: 0.000138mmHg at 25°C
• Refractive Index: 1.768
• CAS DataBase Reference: 1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one(5417-83-4)
• EPA Substance Registry System: 1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one(5417-83-4)

Safety Data

• Hazardous Substances Data: 5417-83-4(Hazardous Substances Data)

Usage

Molecular Structure

1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one has a complex molecular structure that includes a pyrazolo[3,4-d]pyrimidin-4-one ring system, a methylsulfanyl substituent at the 6-position, and a methyl group at the 1-position.

Ring System

The compound contains a pyrazolo[3,4-d]pyrimidin-4-one ring system, which is a fusion of a pyrazole and a pyrimidine ring.

Methyl Group

A methyl group is attached to the 1-position of the molecule, contributing to its structure and properties.

Methylsulfanyl Substituent

A methylsulfanyl group is attached to the 6-position of the molecule, adding sulfur to the structure and potentially influencing its reactivity and interactions with other molecules.

Potential Pharmaceutical Applications

Due to its unique structure, 1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one may have potential pharmaceutical or biological applications.

Building Block for Synthesis

The compound could be used as a building block in the synthesis of other compounds, allowing for the creation of new molecules with various properties and applications.

Starting Point for Drug Development

As a unique chemical structure, it could serve as a starting point for the development of new drugs, potentially leading to the discovery of novel therapeutic agents.

Need for Further Research

To fully understand the properties and potential uses of 1-methyl-6-(methylsulfanyl)-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one, further research and studies are needed. This includes exploring its chemical reactivity, stability, and interactions with other molecules, as well as its potential biological activity and therapeutic applications.

Upstream product

• 5334-27-0 1-methyl-6-thioxo-1,5,6,7-tetrahydro-pyrazolo[3,4-d]pyrimidin-4-one 
• 77-78-1 dimethyl sulfate 
• 18213-75-7 5-amino-1-methyl-1H-pyrazole-4-carboxylic acid amide 
• 70011-76-6 1-methyl-4,6-dimethylthiopyrazolo[3,4-d]pyrimidine 
• 74-88-4 methyl iodide 
• 5334-35-0 6-chloro-1-methyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one 
• 31037-02-2 ethyl 5-amino-1-methyl-1H-pyrazole-4-carboxylate 
• 5334-27-0 1-methyl-6-sulfanyl-5H-pyrazolo[3,4-d]pyrimidin-4-one 

Downstream Products

• 223464-75-3 5-benzyl-1-methyl-6-methylsulfanyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one 
• 1616414-42-6 (3S)-4-[6-(2-hydroxyethylamino)-1-methylpyrazolo[3,4-d]pyrimidin-4-yl]-N-(4-methoxy-2-methylphenyl)-3-methylpiperazine-1-carboxamide 
• 223464-77-5 5-benzyl-6-methanesulfonyl-1-methyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one 
• 223464-86-6 5-benzyl-1-methyl-1,7-dihydro-pyrazolo[3,4-d]pyrimidine-4,6-dione 

Relevant articles and documents

BICYCLIC HETEROCYCLIC COMPOUNDS AS INHIBITORS OFBCDIN3D ACTIVITY

The present invention relates to compounds that function as inhibitors and/or degraders of BCDIN3D activity. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to the

Studies in nucleosides: Part XXI-synthesis of 1/2-substituted-4-amino/hydroxy-6-methylthic-1H/2H-pyrazolo [3,4-d]pyrimidines as analogs of allopurinol and their antileishmanial activity

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