1,2-Ethanediamine, 1,2-bis(2-methoxyphenyl)-, (1S,2S)-

98%

Reagent Code: #65700
fingerprint
CAS Number 148240-65-7

science Other reagents with same CAS 148240-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.34 g/mol
Formula C₁₆H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD17013980
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its structure, featuring methoxy groups and a specific stereochemistry, makes it effective in inducing enantioselectivity, particularly in the formation of chiral centers during organic transformations. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the production of a single enantiomer is crucial for biological activity or product efficacy. Additionally, its application extends to coordination chemistry, where it forms complexes with transition metals, enhancing their catalytic properties in various chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,250.00
inventory 250mg
10-20 days ฿8,982.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,2-Ethanediamine, 1,2-bis(2-methoxyphenyl)-, (1S,2S)-
No image available

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its structure, featuring methoxy groups and a specific stereochemistry, makes it effective in inducing enantioselectivity, particularly in the formation of chiral centers during organic transformations. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the production of a single enantiomer is crucial for biological activity o

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its structure, featuring methoxy groups and a specific stereochemistry, makes it effective in inducing enantioselectivity, particularly in the formation of chiral centers during organic transformations. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the production of a single enantiomer is crucial for biological activity or product efficacy. Additionally, its application extends to coordination chemistry, where it forms complexes with transition metals, enhancing their catalytic properties in various chemical 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...