(S)-4-Ethyl-4-hydroxy-7,8-dihydro-1H-pyrano[3,4-f]indolizine-3,6,10(4H)-trione

95%

Reagent Code: #235611
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CAS Number 110351-94-5

science Other reagents with same CAS 110351-94-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.25 g/mol
Formula C₁₃H₁₃NO₅
badge Registry Numbers
MDL Number MFCD17011873
thermostat Physical Properties
Boiling Point 666.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of indolizine-based bioactive compounds. Shows potential in the development of antitumor and antimicrobial agents due to its structural similarity to naturally occurring alkaloids with demonstrated biological activity. Its unique stereochemistry enhances selectivity in receptor binding studies, making it valuable in drug design for central nervous system disorders. Also employed in studies exploring enzyme inhibition, particularly in kinases and oxidoreductases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,250.00
250mg
10-20 days ฿2,540.00
1g
10-20 days ฿8,090.00
5g
10-20 days ฿29,930.00
25g
10-20 days ฿120,000.00
(S)-4-Ethyl-4-hydroxy-7,8-dihydro-1H-pyrano[3,4-f]indolizine-3,6,10(4H)-trione
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Used in pharmaceutical research as a key intermediate in the synthesis of indolizine-based bioactive compounds. Shows potential in the development of antitumor and antimicrobial agents due to its structural similarity to naturally occurring alkaloids with demonstrated biological activity. Its unique stereochemistry enhances selectivity in receptor binding studies, making it valuable in drug design for central nervous system disorders. Also employed in studies exploring enzyme inhibition, particularly in

Used in pharmaceutical research as a key intermediate in the synthesis of indolizine-based bioactive compounds. Shows potential in the development of antitumor and antimicrobial agents due to its structural similarity to naturally occurring alkaloids with demonstrated biological activity. Its unique stereochemistry enhances selectivity in receptor binding studies, making it valuable in drug design for central nervous system disorders. Also employed in studies exploring enzyme inhibition, particularly in kinases and oxidoreductases.

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