3-Bromo-7-nitro-1H-indazole
98%
Reagent
Code: #118069
CAS Number
74209-34-0
blur_circular Chemical Specifications
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Molecular Information
Weight
242.03 g/mol
Formula
C₇H₄BrN₃O₂
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Registry Numbers
MDL Number
MFCD00159910
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Physical Properties
Boiling Point
248.9°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
This compound is primarily used in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition and receptor modulation. Its structure is valuable in the creation of potential therapeutic agents for treating diseases such as cancer, inflammation, and neurological disorders. Additionally, it is utilized in organic chemistry as a building block for constructing complex heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. Its nitro and bromo functional groups make it a versatile reagent for further chemical modifications.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Light yellow to yellow-brown powder or crystals |
Purity (%) | 97.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
shopping_cart Available Sizes & Pricing
3-Bromo-7-nitro-1H-indazole
This compound is primarily used in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition and receptor modulation. Its structure is valuable in the creation of potential therapeutic agents for treating diseases such as cancer, inflammation, and neurological disorders. Additionally, it is utilized in organic chemistry as a building block for constructing complex heterocyclic compounds, which are essential in drug discovery and medicinal chemistry. Its nitro and bromo functional groups make it a versatile reagent for further chemical modifications.
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