(R)-(-)-BNP acid

98%

Reagent Code: #113884
label
Alias (R)-(-)-Binaphthol Phosphate ; R-Binaphthol Phosphate
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CAS Number 39648-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.29 g/mol
Formula C₂₀H₁₃O₄P
badge Registry Numbers
MDL Number MFCD00010045
thermostat Physical Properties
Melting Point ≥300 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

(R)-(-)-BNP acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the preparation of various bioactive compounds, particularly in the development of enantioselective drugs. Its application is significant in the synthesis of complex molecules where stereochemistry plays a crucial role in biological activity. Additionally, it is employed in the study of enzyme mechanisms and receptor interactions, aiding in the design of more effective and selective therapeutic agents. The compound’s chiral nature makes it valuable in asymmetric synthesis, contributing to the production of optically pure substances.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Powder Or Crystals
Purity (HPLC) 97.5-100
Solubility in Methanol Almost Transparency
Infrared Spectrum Conforms To Structure
Specific Rotation -610 to -590
Specific Rotation -610 to -590

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿370.00
inventory 5g
10-20 days ฿800.00
inventory 25g
10-20 days ฿2,800.00
inventory 100g
10-20 days ฿9,470.00
(R)-(-)-BNP acid
(R)-(-)-BNP acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block for the preparation of various bioactive compounds, particularly in the development of enantioselective drugs. Its application is significant in the synthesis of complex molecules where stereochemistry plays a crucial role in biological activity. Additionally, it is employed in the study of enzyme mechanisms and receptor interactions, aiding in the design of more effective and selective therapeutic agents. The compound’s chiral nature makes it valuable in asymmetric synthesis, contributing to the production of optically pure substances.
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