(1R,2R)-1,2-Bis(2,4,6-trimethoxyphenyl)ethylenediamine Dihydrochloride
93%
- Product Code: 69053
CAS:
1055301-18-2
| Molecular Weight: | 465.37 g./mol | Molecular Formula: | C₂₀H₂₈N₂O₆₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953700 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, in an inert gas |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral ligand in transition metal-catalyzed processes, enabling the production of optically active compounds with high selectivity. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of chiral drugs and intermediates. Additionally, it is employed in organic chemistry research to develop new methodologies for stereocontrolled transformations. The compound's ability to induce chirality makes it valuable for creating complex molecular structures with precise stereochemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Orange to Green powder to crystal |
| PURITY | 93-100 |
| Specific rotation 20Dc1 MeOH | 71-+75 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿1,660.00 |
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(1R,2R)-1,2-Bis(2,4,6-trimethoxyphenyl)ethylenediamine Dihydrochloride
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral ligand in transition metal-catalyzed processes, enabling the production of optically active compounds with high selectivity. Its application is significant in the pharmaceutical industry, where it aids in the synthesis of chiral drugs and intermediates. Additionally, it is employed in organic chemistry research to develop new methodologies for stereocontrolled transformations. The compound's ability to induce chirality makes it valuable for creating complex molecular structures with precise stereochemistry.
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