Cabraleahydroxylactone

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Reagent Code: #161532
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CAS Number 35833-69-3

science Other reagents with same CAS 35833-69-3

blur_circular Chemical Specifications

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Weight 417 g/mol
Formula C₂₇H₄₄O₃
inventory_2 Storage & Handling
Storage 2-8℃, dry, closed

description Product Description

Used in advanced organic synthesis as a chiral building block for natural product synthesis, particularly in the development of bioactive lactone derivatives. Shows potential in pharmaceutical research due to its structural similarity to compounds with antimicrobial and anti-inflammatory properties. Also employed as a reagent in stereoselective reactions, aiding in the formation of complex cyclic frameworks found in terpenoids and polyketide-like molecules. Its hydroxylactone functionality allows for further functionalization, making it valuable in medicinal chemistry for scaffold diversification.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿25,730.00

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Cabraleahydroxylactone
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Used in advanced organic synthesis as a chiral building block for natural product synthesis, particularly in the development of bioactive lactone derivatives. Shows potential in pharmaceutical research due to its structural similarity to compounds with antimicrobial and anti-inflammatory properties. Also employed as a reagent in stereoselective reactions, aiding in the formation of complex cyclic frameworks found in terpenoids and polyketide-like molecules. Its hydroxylactone functionality allows for fur

Used in advanced organic synthesis as a chiral building block for natural product synthesis, particularly in the development of bioactive lactone derivatives. Shows potential in pharmaceutical research due to its structural similarity to compounds with antimicrobial and anti-inflammatory properties. Also employed as a reagent in stereoselective reactions, aiding in the formation of complex cyclic frameworks found in terpenoids and polyketide-like molecules. Its hydroxylactone functionality allows for further functionalization, making it valuable in medicinal chemistry for scaffold diversification.

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