tert-Butyl (trans-3-formylcyclobutyl)carbamate

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Reagent Code: #141088
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CAS Number 171549-92-1

science Other reagents with same CAS 171549-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.2462 g/mol
Formula C₁₀H₁₇NO₃
badge Registry Numbers
MDL Number MFCD28403246
thermostat Physical Properties
Boiling Point 304.8±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.07±0.1 g/cm3(Predicted)
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules that require cyclobutane-based scaffolds. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or Wittig transformations, enabling the construction of complex amine-containing structures. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity and stability under various reaction conditions. Commonly employed in medicinal chemistry for optimizing drug candidates targeting CNS disorders and metabolic diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,650.00
inventory 500mg
10-20 days ฿17,880.00

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tert-Butyl (trans-3-formylcyclobutyl)carbamate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules that require cyclobutane-based scaffolds. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or Wittig transformations, enabling the construction of complex amine-containing structures. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity and stabil
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules that require cyclobutane-based scaffolds. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or Wittig transformations, enabling the construction of complex amine-containing structures. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity and stability under various reaction conditions. Commonly employed in medicinal chemistry for optimizing drug candidates targeting CNS disorders and metabolic diseases.
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