(1R,2R)-N-p-Tosyl-1,2-cyclohexanediamine
97%
- Product Code: 70804
CAS:
174291-96-4
| Molecular Weight: | 268.4 g./mol | Molecular Formula: | C₁₃H₂₀N₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 105-109°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. It plays a significant role in enantioselective reactions, such as hydrogenation and carbon-carbon bond formation, where high stereochemical control is required. Additionally, it is employed in the synthesis of pharmaceuticals and fine chemicals, where its chiral structure helps in producing optically active compounds with high purity. Its tosyl group also facilitates further functionalization, making it a versatile intermediate in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft20,255.32 |
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| 5.000 | 10-20 days | Ft80,590.33 |
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(1R,2R)-N-p-Tosyl-1,2-cyclohexanediamine
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. It plays a significant role in enantioselective reactions, such as hydrogenation and carbon-carbon bond formation, where high stereochemical control is required. Additionally, it is employed in the synthesis of pharmaceuticals and fine chemicals, where its chiral structure helps in producing optically active compounds with high purity. Its tosyl group also facilitates further functionalization, making it a versatile intermediate in organic synthesis.
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