(R)-2-((tert-Butoxycarbonyl)amino)-2-phenylethyl methanesulfonate

98%

Reagent Code: #113474
fingerprint
CAS Number 102089-75-8

science Other reagents with same CAS 102089-75-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.39 g/mol
Formula C₁₄H₂₁NO₅S
badge Registry Numbers
MDL Number MFCD22571103
thermostat Physical Properties
Melting Point 112-114 °C
Boiling Point 497.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.204±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily used in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where the (R)-configuration is essential for biological activity. Its methanesulfonate group makes it a suitable substrate for nucleophilic substitution reactions, enabling the introduction of various functional groups. Additionally, it is utilized in peptide coupling reactions, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, ensuring selective reactions in complex molecular constructions. Its application is critical in the development of targeted therapies and bioactive molecules.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE White to off-white solid
Purity (%) 97.5-100
OR(C=1.00g/100ml CHCL3) -24.5--20.5
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿3,861.00
inventory 5g
10-20 days ฿342.00
inventory 25g
10-20 days ฿1,170.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-((tert-Butoxycarbonyl)amino)-2-phenylethyl methanesulfonate
No image available
This chemical is primarily used in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where the (R)-configuration is essential for biological activity. Its methanesulfonate group makes it a suitable substrate for nucleophilic substitution reactions, enabling the introduction of various functional groups. Additionally, it is utilized in peptide coupling reactions, where the tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, ensuring selective reactions in complex molecular constructions. Its application is critical in the development of targeted therapies and bioactive molecules.
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...