(R)-Benzyl 2-amino-3-(4-hydroxyphenyl)propanoate 4-methylbenzenesulfonate

≥95%

Reagent Code: #51860
fingerprint
CAS Number 97984-63-9

science Other reagents with same CAS 97984-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 443.51 g/mol
Formula C₂₃H₂₅NO₆S
badge Registry Numbers
MDL Number MFCD00136658
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral drugs. Its structure, featuring a hydroxyphenyl group and an amino acid ester, makes it valuable for developing medications targeting neurological and cardiovascular conditions. It is often employed in the production of enantiomerically pure compounds, ensuring high specificity and efficacy in drug formulations. Additionally, it serves as a key building block in the creation of peptide-based therapeutics, where its stereochemistry plays a critical role in biological activity.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿18,280.00
inventory 1g
10-20 days ฿1,020.00
inventory 5g
10-20 days ฿4,360.00
inventory 10g
10-20 days ฿7,820.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-Benzyl 2-amino-3-(4-hydroxyphenyl)propanoate 4-methylbenzenesulfonate
No image available
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of chiral drugs. Its structure, featuring a hydroxyphenyl group and an amino acid ester, makes it valuable for developing medications targeting neurological and cardiovascular conditions. It is often employed in the production of enantiomerically pure compounds, ensuring high specificity and efficacy in drug formulations. Additionally, it serves as a key building block in the creation of peptide-based therapeutics, where its stereochemistry plays a critical role in biological activity.
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...