tert-butyl N-[(1R)-3-oxocyclohexyl]carbamate

98%

Reagent Code: #219535
fingerprint
CAS Number 1383797-87-2

science Other reagents with same CAS 1383797-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.27 g/mol
Formula C₁₁H₁₉NO₃
badge Registry Numbers
MDL Number MFCD30181863
thermostat Physical Properties
Boiling Point 335.9±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.06±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals. It serves as a protected amine building block in the construction of complex molecules, especially in the synthesis of bioactive compounds containing cyclohexyl or cyclohexanone frameworks. The tert-butyl carbamate (Boc) group provides stability during reaction sequences and can be easily removed under mild acidic conditions, allowing for selective deprotection and further functionalization. Its chiral center makes it valuable in asymmetric synthesis, where stereochemical control is critical for drug efficacy. Commonly employed in medicinal chemistry for the preparation of enzyme inhibitors and central nervous system agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,780.00
inventory 250mg
10-20 days ฿9,020.00
inventory 1g
10-20 days ฿21,340.00
tert-butyl N-[(1R)-3-oxocyclohexyl]carbamate
No image available

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals. It serves as a protected amine building block in the construction of complex molecules, especially in the synthesis of bioactive compounds containing cyclohexyl or cyclohexanone frameworks. The tert-butyl carbamate (Boc) group provides stability during reaction sequences and can be easily removed under mild acidic conditions, allowing for selective deprotection and further functionalization. Its chiral cente

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals. It serves as a protected amine building block in the construction of complex molecules, especially in the synthesis of bioactive compounds containing cyclohexyl or cyclohexanone frameworks. The tert-butyl carbamate (Boc) group provides stability during reaction sequences and can be easily removed under mild acidic conditions, allowing for selective deprotection and further functionalization. Its chiral center makes it valuable in asymmetric synthesis, where stereochemical control is critical for drug efficacy. Commonly employed in medicinal chemistry for the preparation of enzyme inhibitors and central nervous system agents.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...