4-Chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine
98%
Reagent
Code: #119175
CAS Number
479633-63-1
blur_circular Chemical Specifications
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Molecular Information
Weight
307.76 g/mol
Formula
C₁₃H₁₀ClN₃O₂S
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Registry Numbers
MDL Number
MFCD09907939
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Storage & Handling
Density
1.49g/cm3
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis and medicinal chemistry as a versatile intermediate for the development of biologically active molecules. Its structure, featuring both a pyrrolo[2,3-d]pyrimidine core and a tosyl group, makes it a valuable building block for constructing more complex heterocyclic compounds. It is often employed in the synthesis of kinase inhibitors, which are crucial in targeting various diseases, including cancer and inflammatory disorders. Additionally, its reactive sites allow for further functionalization, enabling researchers to tailor its properties for specific applications in drug discovery and development. The compound’s stability and reactivity make it a preferred choice in the design and optimization of pharmaceutical agents.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (%) | 98-100% |
Melting Point (°C) | 145-155 |
Infrared Spectrum | Conforms To Structure |
Appearance | Yellow To Brown Solid Or Powder |
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4-Chloro-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine
This compound is primarily utilized in organic synthesis and medicinal chemistry as a versatile intermediate for the development of biologically active molecules. Its structure, featuring both a pyrrolo[2,3-d]pyrimidine core and a tosyl group, makes it a valuable building block for constructing more complex heterocyclic compounds. It is often employed in the synthesis of kinase inhibitors, which are crucial in targeting various diseases, including cancer and inflammatory disorders. Additionally, its reactive sites allow for further functionalization, enabling researchers to tailor its properties for specific applications in drug discovery and development. The compound’s stability and reactivity make it a preferred choice in the design and optimization of pharmaceutical agents.
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