(S)-3,3'-Dibromo-2,2'-dimethoxy-1,1'-binaphthyl

98.0%

Reagent Code: #66361
fingerprint
CAS Number 75714-60-2

science Other reagents with same CAS 75714-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 472.18 g/mol
Formula C₂₂H₁₆Br₂O₂
badge Registry Numbers
MDL Number MFCD04038415
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a significant role in the formation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the development of drugs with specific chiral configurations. Its structure allows it to effectively coordinate with metal catalysts, enhancing the selectivity and efficiency of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Additionally, it is employed in the synthesis of complex organic molecules, contributing to advancements in material science and fine chemical production. Its chiral properties make it a valuable tool in research and industrial applications where precise stereochemical control is required.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 180-185
Purity (GC) 98-100%
Specific Rotation [α]20/D (CHCl3) -10 to 0
Infrared Spectrometry Conforms to Structure
Solubility in Chloroform Almost transparent

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,011.00
inventory 250mg
10-20 days ฿3,159.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-3,3'-Dibromo-2,2'-dimethoxy-1,1'-binaphthyl
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a significant role in the formation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the development of drugs with specific chiral configurations. Its structure allows it to effectively coordinate with metal catalysts, enhancing the selectivity and efficiency of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation pro

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a significant role in the formation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the development of drugs with specific chiral configurations. Its structure allows it to effectively coordinate with metal catalysts, enhancing the selectivity and efficiency of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Additionally, it is employed in the synthesis of complex organic molecules, contributing to advancements in material science and fine chemical production. Its chiral properties make it a valuable tool in research and industrial applications where precise stereochemical control is required.

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...