Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate

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Reagent Code: #119037
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CAS Number 72817-85-7

science Other reagents with same CAS 72817-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.22 g/mol
Formula C₁₁H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD02089547
thermostat Physical Properties
Boiling Point 433.9±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily used in the synthesis of advanced organic compounds, particularly in the development of pharmaceutical intermediates. It serves as a key building block in the creation of various heterocyclic compounds, which are essential in drug discovery and development. Its structure allows for versatile modifications, making it valuable in the production of potential therapeutic agents, including anti-inflammatory and antimicrobial drugs. Additionally, it is employed in research laboratories for studying chemical reactions and developing novel synthetic pathways in organic chemistry.

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Test Parameter Specification
Appearance Off-white To Yellow Powder Or Crystals
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,800.00
inventory 250mg
10-20 days ฿14,600.00

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Ethyl 4-amino-5-cyano-2-hydroxy-3-methylbenzoate
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This chemical is primarily used in the synthesis of advanced organic compounds, particularly in the development of pharmaceutical intermediates. It serves as a key building block in the creation of various heterocyclic compounds, which are essential in drug discovery and development. Its structure allows for versatile modifications, making it valuable in the production of potential therapeutic agents, including anti-inflammatory and antimicrobial drugs. Additionally, it is employed in research laboratories for studying chemical reactions and developing novel synthetic pathways in organic chemistry.
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