(S)-tert-Butyl but-3-yn-2-ylcarbamate

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Reagent Code: #113843
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CAS Number 118080-79-8

science Other reagents with same CAS 118080-79-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.22 g/mol
Formula C₉H₁₅NO₂
badge Registry Numbers
MDL Number MFCD18835704
thermostat Physical Properties
Boiling Point 235.4±23.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and biologically active molecules. Its structure, featuring a tert-butyl carbamate group and an alkyne moiety, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in asymmetric synthesis to introduce chiral centers into target compounds. Additionally, the alkyne group allows for further functionalization through reactions like click chemistry or coupling reactions, enabling the development of diverse chemical structures. Its stability and reactivity make it a useful intermediate in medicinal chemistry for designing drug candidates with specific stereochemical properties.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,470.00
inventory 100mg
10-20 days ฿3,735.00

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(S)-tert-Butyl but-3-yn-2-ylcarbamate
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This compound is primarily utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and biologically active molecules. Its structure, featuring a tert-butyl carbamate group and an alkyne moiety, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in asymmetric synthesis to introduce chiral centers into target compounds. Additionally, the alkyne group allows for further functionalization through reactions like click chemistry or coupling reactions, enabling the development of diverse chemical structures. Its stability and reactivity make it a useful intermediate in medicinal chemistry for designing drug candidates with specific stereochemical properties.
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