tert-Butyl ((1R,2S)-2-hydroxycyclopentyl)carbamate

98%

Reagent Code: #229476
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CAS Number 1330069-67-4

science Other reagents with same CAS 1330069-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD14155660
thermostat Physical Properties
Boiling Point 320.8±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.08±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral cyclopentyl backbone and protected amine group make it valuable in constructing enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for optimizing drug candidates targeting metabolic and neurological disorders. The tert-butyl carbamate (Boc) group allows for selective amine protection during multi-step syntheses, enhancing reaction specificity and yield.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,450.00
inventory 250mg
10-20 days ฿13,000.00
inventory 1g
10-20 days ฿31,200.00
tert-Butyl ((1R,2S)-2-hydroxycyclopentyl)carbamate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral cyclopentyl backbone and protected amine group make it valuable in constructing enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for optimizing drug candidates targeting metabolic and neurological disorders. The tert-butyl carbamate (Boc) group allows for selective amine protection during multi-step syntheses, enhancing reaction speci

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral cyclopentyl backbone and protected amine group make it valuable in constructing enzyme inhibitors and receptor modulators. Commonly employed in medicinal chemistry for optimizing drug candidates targeting metabolic and neurological disorders. The tert-butyl carbamate (Boc) group allows for selective amine protection during multi-step syntheses, enhancing reaction specificity and yield.

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