(R)-tert-Butyl (4-oxobutan-2-yl)carbamate

97%

Reagent Code: #113419
fingerprint
CAS Number 497861-77-5

science Other reagents with same CAS 497861-77-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₉H₁₇NO₃
badge Registry Numbers
MDL Number MFCD18835622
thermostat Physical Properties
Boiling Point 279.9±23.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, store under inert gas

description Product Description

This chemical is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its application is significant in the development of drugs that require precise chiral configurations to achieve desired therapeutic effects. Additionally, it is employed in organic synthesis for constructing complex molecules, often in the preparation of peptidomimetics or other biologically active compounds. Its role in asymmetric synthesis makes it valuable for creating enantiomerically pure substances, which are essential in modern drug discovery and development processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿1,512.00
inventory 100mg
10-20 days ฿3,780.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-tert-Butyl (4-oxobutan-2-yl)carbamate
No image available
This chemical is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its application is significant in the development of drugs that require precise chiral configurations to achieve desired therapeutic effects. Additionally, it is employed in organic synthesis for constructing complex molecules, often in the preparation of peptidomimetics or other biologically active compounds. Its role in asymmetric synthesis makes it valuable for creating enantiomerically pure substances, which are essential in modern drug discovery and development processes.
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...