11,12-Didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-yl 4-nitrophenyl carbonate

95%

Reagent Code: #133768
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CAS Number 1027338-09-5

science Other reagents with same CAS 1027338-09-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 385.37 g/mol
Formula C₂₃H₁₅NO₅
badge Registry Numbers
MDL Number MFCD32669778
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used in organic synthesis as a highly specialized reagent for selective hydroxyl protection and deprotection strategies. Its unique polycyclic structure enables steric control in complex molecule assembly, particularly in the preparation of natural product derivatives and pharmaceutical intermediates. The 4-nitrophenyl carbonate moiety acts as a good leaving group, facilitating nucleophilic substitution under mild conditions. Commonly employed in the development of enzyme inhibitors and prodrug systems where controlled release of active alcohols or phenols is required. Also utilized in polymer chemistry for cross-linking agents due to its bifunctional reactivity and rigid backbone.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿13,240.00
inventory 100mg
10-20 days ฿25,940.00

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11,12-Didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-yl 4-nitrophenyl carbonate
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Used in organic synthesis as a highly specialized reagent for selective hydroxyl protection and deprotection strategies. Its unique polycyclic structure enables steric control in complex molecule assembly, particularly in the preparation of natural product derivatives and pharmaceutical intermediates. The 4-nitrophenyl carbonate moiety acts as a good leaving group, facilitating nucleophilic substitution under mild conditions. Commonly employed in the development of enzyme inhibitors and prodrug systems w

Used in organic synthesis as a highly specialized reagent for selective hydroxyl protection and deprotection strategies. Its unique polycyclic structure enables steric control in complex molecule assembly, particularly in the preparation of natural product derivatives and pharmaceutical intermediates. The 4-nitrophenyl carbonate moiety acts as a good leaving group, facilitating nucleophilic substitution under mild conditions. Commonly employed in the development of enzyme inhibitors and prodrug systems where controlled release of active alcohols or phenols is required. Also utilized in polymer chemistry for cross-linking agents due to its bifunctional reactivity and rigid backbone.

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