(1S,2S)-N1,N1,N2,N2-Tetramethyl-1,2-diphenylethane-1,2-diamine
97%
- Product Code: 87033
CAS:
91361-07-8
| Molecular Weight: | 268.40 g./mol | Molecular Formula: | C₁₈H₂₄N₂ |
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| EC Number: | MDL Number: | MFCD06797770 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored under 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 for the synthesis of chiral drugs, where the precise control of stereochemistry is crucial. Additionally, it is employed in the development of advanced materials and fine chemicals, contributing to the creation of complex molecular architectures with specific stereochemical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $19.17 |
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| 0.100 | 10-20 days | $32.94 |
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| 0.250 | 10-20 days | $62.38 |
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(1S,2S)-N1,N1,N2,N2-Tetramethyl-1,2-diphenylethane-1,2-diamine
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 for the synthesis of chiral drugs, where the precise control of stereochemistry is crucial. Additionally, it is employed in the development of advanced materials and fine chemicals, contributing to the creation of complex molecular architectures with specific stereochemical properties.
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