(S)-tert-Butyl 1-aminopropan-2-ylcarbamate

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Reagent Code: #82988
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CAS Number 146552-71-8

science Other reagents with same CAS 146552-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.24 g/mol
Formula C₈H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD08726031
thermostat Physical Properties
Boiling Point 264°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in the pharmaceutical and chemical synthesis industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly in the synthesis of chiral compounds. Its structure allows it to act as a protecting group for amines during complex chemical reactions, ensuring selective transformations. Additionally, it is employed in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Its chiral nature makes it valuable in creating enantiomerically pure substances, which are critical for the efficacy and safety of many medications.

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Test Parameter Specification
Appearance Light brown to brown 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 100mg
10-20 days ฿1,980.00
inventory 250mg
10-20 days ฿3,180.00
inventory 1g
10-20 days ฿8,240.00
inventory 5g
10-20 days ฿26,847.00

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(S)-tert-Butyl 1-aminopropan-2-ylcarbamate
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This compound is primarily used in the pharmaceutical and chemical synthesis industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly in the synthesis of chiral compounds. Its structure allows it to act as a protecting group for amines during complex chemical reactions, ensuring selective transformations. Additionally, it is employed in the development of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Its chiral nature makes it valuable in creating enantiomerically pure substances, which are critical for the efficacy and safety of many medications.
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