N-Boc-8-hydroxy-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine-7-carbaldehyde

≥95%

Reagent Code: #172984
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CAS Number 1823551-73-0

science Other reagents with same CAS 1823551-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.32 g/mol
Formula C₁₅H₁₉NO₅
badge Registry Numbers
MDL Number MFCD28101612
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting central nervous system disorders. Its structure allows for selective modifications, making it valuable in developing serotonin receptor modulators. The aldehyde and hydroxy groups enable further functionalization through reactions like reductive amination, Wittig chemistry, or etherification, while the Boc-protected scaffold ensures stability during multi-step syntheses. Commonly employed in medicinal chemistry for constructing novel heterocyclic systems with potential therapeutic effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿30,950.00
inventory 1g
10-20 days ฿83,610.00

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N-Boc-8-hydroxy-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine-7-carbaldehyde
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting central nervous system disorders. Its structure allows for selective modifications, making it valuable in developing serotonin receptor modulators. The aldehyde and hydroxy groups enable further functionalization through reactions like reductive amination, Wittig chemistry, or etherification, while the Boc-protected scaffold ensures stability during multi-step syntheses. Commonly e
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting central nervous system disorders. Its structure allows for selective modifications, making it valuable in developing serotonin receptor modulators. The aldehyde and hydroxy groups enable further functionalization through reactions like reductive amination, Wittig chemistry, or etherification, while the Boc-protected scaffold ensures stability during multi-step syntheses. Commonly employed in medicinal chemistry for constructing novel heterocyclic systems with potential therapeutic effects.
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