100047-42-5

Basic information

• Product Name: 6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one
• Synonyms: 6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one;1,2-Dihydro-6-(methylthio)-3H-pyrazolo[3,4-d]pyrimidin-3-one;6-Methylsulfanyl-1,2-dihydro-pyrazolo[3,4-d]pyrimidin-3-one
• CAS NO: 100047-42-5
• Molecular Formula: C₆H₆N₄OS
• Molecular Weight: 182.20304
• Mol File: 100047-42-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.78
• CAS DataBase Reference: 6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one(100047-42-5)
• EPA Substance Registry System: 6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one(100047-42-5)

Safety Data

• Hazardous Substances Data: 100047-42-5(Hazardous Substances Data)

Usage

General Description

6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one is a chemical compound with the molecular formula C7H7N3OS. It is a heterocyclic compound with a pyrazolopyrimidine structure, and it contains a methylthio group. 6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one has potential pharmaceutical applications and may be used as a building block in the synthesis of other organic compounds. Its specific properties and potential uses may vary depending on the particular application and context, and further research may be necessary to fully understand its potential uses and limitations.

Upstream product

• 117147-06-5 ethyl 4-hydrazinyl-2-(methylsulfanyl)pyrimidine-5-carboxylate 
• 5909-24-0 4-chloro-2-methanesulfanylpyrimidine-5-carboxylic acid ethyl ester 

Downstream Products

• 1306830-00-1 1-cyclohexyl-3-phenyl-N-propyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine 
• 1306830-01-2 C₂₁H₂₅N₅O₂ 
• 1306830-02-3 C₂₂H₂₇N₅O₂ 
• 1306830-03-4 C₁₈H₂₃N₅O 
• 1306830-05-6 tert-butyl 4-((3-(2-methoxyphenyl)-6-(propylamino)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)piperidine-1-carboxylate 
• 1306830-06-7 C₂₁H₂₈N₆O 
• 1306829-95-7 3-bromo-6-(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine 
• 1306830-08-9 C₂₂H₂₀N₆ 
• 1306830-10-3 1-isopropyl-3-phenyl-N-propyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine 
• 1306830-11-4 C₁₈H₂₁N₅ 
• 1306830-12-5 C₁₆H₁₉N₅ 
• 1306830-13-6 C₁₉H₁₉N₅O 
• 1306830-14-7 1-isopropyl-N,3-diphenyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine 
• 1306830-15-8 C₂₁H₂₁N₅O 

Relevant articles and documents

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Microwave-assisted, divergent solution-phase synthesis of 1,3,6-trisubstituted pyrazolo[3,4- d ]pyrimidines

A concise and highly divergent synthetic route has been developed to rapidly access 1,3,6-trisubstituted pyrazolopyrimidines. The synthesis features a microwave assisted one-pot N1-alkylation/Suzuki-Miyaura reaction as the key step. The sequence of the synthetic scheme can be varied to selectively modify the N1, C3, or C6 position at a late synthetic stage, thereby providing a highly efficient approach to explore the structure-activity relationships of pyrazolopyrimidine derivatives. The scope of these reactions has also been explored.