(2S,3S,4R,5R,6R)-2-(3-(4-Acetoxybenzyl)-4-chlorophenyl)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyltriacetate

98%

Reagent Code: #237889
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CAS Number 912917-85-2

science Other reagents with same CAS 912917-85-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 591.00 g/mol
Formula C₂₉H₃₁ClO₁₁
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of certain pharmaceutical compounds, particularly in the development of selective estrogen receptor modulators (SERMs). Its functional groups and stereochemistry make it valuable for constructing complex drug molecules with high specificity. Commonly employed in research settings for modifying bioactive compounds to enhance stability, bioavailability, or receptor binding affinity. Also utilized in the preparation of prodrugs where controlled release of active agents is required. Its acetyl-protected hydroxyl groups allow for stepwise deprotection and further chemical modifications in multi-step organic syntheses.

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inventory 10mg
10-20 days ฿203,280.00

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(2S,3S,4R,5R,6R)-2-(3-(4-Acetoxybenzyl)-4-chlorophenyl)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyltriacetate
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Used as a key intermediate in the synthesis of certain pharmaceutical compounds, particularly in the development of selective estrogen receptor modulators (SERMs). Its functional groups and stereochemistry make it valuable for constructing complex drug molecules with high specificity. Commonly employed in research settings for modifying bioactive compounds to enhance stability, bioavailability, or receptor binding affinity. Also utilized in the preparation of prodrugs where controlled release of active a

Used as a key intermediate in the synthesis of certain pharmaceutical compounds, particularly in the development of selective estrogen receptor modulators (SERMs). Its functional groups and stereochemistry make it valuable for constructing complex drug molecules with high specificity. Commonly employed in research settings for modifying bioactive compounds to enhance stability, bioavailability, or receptor binding affinity. Also utilized in the preparation of prodrugs where controlled release of active agents is required. Its acetyl-protected hydroxyl groups allow for stepwise deprotection and further chemical modifications in multi-step organic syntheses.

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