2-Amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

≥95%

Reagent Code: #42674
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CAS Number 99907-84-3

science Other reagents with same CAS 99907-84-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.28 g/mol
Formula C₁₃H₁₇NO₄
badge Registry Numbers
MDL Number MFCD15529610
thermostat Physical Properties
Boiling Point 476.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.24 g/cm3
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting neurological and cardiovascular disorders. Its structural features make it suitable for constructing complex heterocyclic compounds, which are often explored for their potential therapeutic properties. Additionally, it is employed in the study of enzyme inhibition and receptor modulation, contributing to the discovery of new drug candidates. Its dimethoxy and carboxylic acid groups enhance its versatility in chemical reactions, allowing for further functionalization and optimization in medicinal chemistry applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,700.00
inventory 250mg
10-20 days ฿8,960.00
inventory 1g
10-20 days ฿22,090.00

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2-Amino-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting neurological and cardiovascular disorders. Its structural features make it suitable for constructing complex heterocyclic compounds, which are often explored for their potential therapeutic properties. Additionally, it is employed in the study of enzyme inhibition and receptor modulation, contributing to the discovery of new drug candidates. Its dimethoxy and carboxylic acid groups enhance its versatility in chemical reactions, allowing for further functionalization and optimization in medicinal chemistry applications.
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