(R)-5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid

≥95%

Reagent Code: #113585
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CAS Number 76093-33-9

science Other reagents with same CAS 76093-33-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.31 g/mol
Formula C₁₆H₁₆N₂O₆
badge Registry Numbers
MDL Number MFCD09952191
thermostat Physical Properties
Boiling Point 505°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.345g/cm3
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of calcium channel blockers. These blockers are crucial in managing cardiovascular conditions such as hypertension and angina by relaxing the muscles of the heart and blood vessels. Additionally, its structural features make it valuable in research for developing new drugs with improved efficacy and reduced side effects. The compound’s specific stereochemistry and functional groups also contribute to its role in studying enzyme interactions and receptor binding mechanisms, aiding in the design of targeted therapies.

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Test Parameter Specification
Appearance Pale yellow to yellow powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,331.00
inventory 5g
10-20 days ฿6,876.00
inventory 10g
10-20 days ฿12,393.00

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(R)-5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of calcium channel blockers. These blockers are crucial in managing cardiovascular conditions such as hypertension and angina by relaxing the muscles of the heart and blood vessels. Additionally, its structural features make it valuable in research for developing new drugs with improved efficacy and reduced side effects. The compound’s specific stereochemistry and functional groups also contribute to its role in studying enzyme interactions and receptor binding mechanisms, aiding in the design of targeted therapies.
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