2-Amino-5-methylnicotinonitrile

98%

Reagent Code: #63339
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CAS Number 38076-78-7

science Other reagents with same CAS 38076-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 133.15 g/mol
Formula C₇H₇N₃
badge Registry Numbers
MDL Number MFCD07779068
thermostat Physical Properties
Boiling Point 310.56°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of compounds with potential therapeutic effects, particularly in the creation of molecules targeting neurological and metabolic disorders. Additionally, it is employed in organic synthesis to construct complex heterocyclic structures, which are often found in drugs with anti-inflammatory, antiviral, or anticancer properties. Its nitrile and amino functional groups make it a versatile building block for further chemical modifications, enabling the production of diverse biologically active molecules.

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Test Parameter Specification
Appearance White to off-white powder or crystals
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,680.00
inventory 250mg
10-20 days ฿5,080.00
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2-Amino-5-methylnicotinonitrile
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This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of compounds with potential therapeutic effects, particularly in the creation of molecules targeting neurological and metabolic disorders. Additionally, it is employed in organic synthesis to construct complex heterocyclic structures, which are often found in drugs with anti-inflammatory, antiviral, or anticancer properties. Its nitrile and amino functional groups make it a versatile building block for further chemical modifications, enabling the production of diverse biologically active molecules.
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