70011-76-6

Basic information

• Product Name: 1-methyl-4,6-bis(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine
• CAS NO: 70011-76-6
• Molecular Formula: C₈H₁₀N₄S₂
• Molecular Weight: 226.3218
• Mol File: 70011-76-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 435.9°C at 760 mmHg
• Flash Point: 217.4°C
• Density: 1.45g/cm³
• Vapor Pressure: 2.15E-07mmHg at 25°C
• Refractive Index: 1.735
• CAS DataBase Reference: 1-methyl-4,6-bis(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-4,6-bis(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine(70011-76-6)
• EPA Substance Registry System: 1-methyl-4,6-bis(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine(70011-76-6)

Safety Data

• Hazardous Substances Data: 70011-76-6(Hazardous Substances Data)

Usage

Chemical Family

pyrazolo[3,4-d]pyrimidine

Explanation

Different sources of media describe the Explanation of 70011-76-6 differently. You can refer to the following data:
1. 1-methyl-4,6-bis(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine belongs to the pyrazolo[3,4-d]pyrimidine family of compounds.
2. It is a pyrimidine derivative, which means it is a modified version of the base pyrimidine structure.
3. The compound has two methylsulfanyl side chains attached to it, which contribute to its chemical properties and potential applications.
4. The methylsulfanyl side chains are specifically attached to the 4 and 6 positions of the pyrazolo ring, which influences the compound's structure and properties.
5. 1-methyl-4,6-bis(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidine has potential applications in pharmaceutical research, particularly in the development of new drugs for various medical conditions.
6. The compound may be used as a building block in organic synthesis to create other related compounds with different properties and applications.
7. Its structure and properties make it a valuable research tool for studying the structure-activity relationships of pyrazolo[3,4-d]pyrimidine derivatives in drug discovery and development.

Derivative

pyrimidine

Side chains

two methylsulfanyl groups

Position of side chains

4 and 6 positions of the pyrazolo ring

Potential applications

pharmaceutical research

Use as a building block

organic synthesis

Research tool

structure-activity relationships

Upstream product

• 30682-70-3 1-methylpyrazolo[3,4-d]pyrimidin-4,6(5H,7H)-dithione 
• 74-88-4 methyl iodide 
• 6288-89-7 4,6-Bis-methylsulfanyl-1H-pyrazolo[3,4-d]pyrimidine 

Downstream Products

• 5417-83-4 1-methyl-6-methylthio-4(5H)-oxo-1H-pyrazolo<3,4-d>pyrimidine 

Relevant articles and documents

Synthesis and antimicrobial activity of some heterocycles: Part-V

Ortho-aminonitrile (1) was prepared from ethoxymethylenemalononitrile. 4-Allylamino-1-methyl-6-methylthiopyrazolo[3,4-d]pyrimidine (4) was prepared by an initial treatment of compound (1) with carbon disulfide in pyridine followed by methylation with methyl iodide and subsequent reaction with allylamine in acetonitrile. Orthoaminoester (5) was prepared from ethyl (ethoxymethylene) cyanoacetate. Reaction of compound (5) with formamide yielded compound (6), which was then tosylated. All compounds were screened for their antibacterial and antifungal activities.