(7a,17a)-17-Hydroxy-3-oxo-pregna-4,9(11)-diene-7,21-dicarboxylate gamma-lactone methyl ester

95%

Reagent Code: #92823
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CAS Number 95716-70-4

science Other reagents with same CAS 95716-70-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.49 g/mol
Formula C₂₄H₃₀O₅
badge Registry Numbers
MDL Number MFCD01244531
thermostat Physical Properties
Boiling Point 580.2ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.24 g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of steroidal drugs, particularly those with anti-inflammatory or hormonal activity. Its unique structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Researchers often employ it in the development of corticosteroids or other therapeutic agents targeting conditions such as arthritis, asthma, or autoimmune disorders. Additionally, its lactone and ester functional groups make it a versatile building block for creating more complex steroid derivatives with tailored biological properties.

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Test Parameter Specification
Appearance Yellow solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,680.00

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(7a,17a)-17-Hydroxy-3-oxo-pregna-4,9(11)-diene-7,21-dicarboxylate gamma-lactone methyl ester
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of steroidal drugs, particularly those with anti-inflammatory or hormonal activity. Its unique structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Researchers often employ it in the development of corticosteroids or other therapeutic agents targeting conditions such as arthritis, asthma, or autoimmune disorders. Additionally, its lactone and ester functional groups make it a versatile building block for creating more complex steroid derivatives with tailored biological properties.
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