5,8,9,14-Tetraacetoxy-3-benzoyloxy-10,15-dihydroxypepluane

95%

Reagent Code: #241413
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CAS Number 219916-77-5

science Other reagents with same CAS 219916-77-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 658.73 g/mol
Formula C₃₅H₄₆O₁₂
badge Registry Numbers
MDL Number MFCD28385987
inventory_2 Storage & Handling
Density 1.31±0.1g/ml
Storage 2-8℃, dry, closed

description Product Description

Used in specialized organic synthesis as a complex polyfunctional intermediate, particularly in the preparation of highly substituted peptidomimetic structures and natural product analogs. Its multiple acetoxy and hydroxy groups allow selective deprotection and conjugation, making it valuable in medicinal chemistry for constructing sterically hindered frameworks. Commonly employed in the development of protease inhibitors and anti-inflammatory agents due to its rigid scaffold and ability to mimic peptide turn motifs. Also utilized in prodrug design where controlled release of active components is achieved through ester hydrolysis in physiological environments.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿37,490.00
5,8,9,14-Tetraacetoxy-3-benzoyloxy-10,15-dihydroxypepluane
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Used in specialized organic synthesis as a complex polyfunctional intermediate, particularly in the preparation of highly substituted peptidomimetic structures and natural product analogs. Its multiple acetoxy and hydroxy groups allow selective deprotection and conjugation, making it valuable in medicinal chemistry for constructing sterically hindered frameworks. Commonly employed in the development of protease inhibitors and anti-inflammatory agents due to its rigid scaffold and ability to mimic peptide

Used in specialized organic synthesis as a complex polyfunctional intermediate, particularly in the preparation of highly substituted peptidomimetic structures and natural product analogs. Its multiple acetoxy and hydroxy groups allow selective deprotection and conjugation, making it valuable in medicinal chemistry for constructing sterically hindered frameworks. Commonly employed in the development of protease inhibitors and anti-inflammatory agents due to its rigid scaffold and ability to mimic peptide turn motifs. Also utilized in prodrug design where controlled release of active components is achieved through ester hydrolysis in physiological environments.

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