(1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)cyclohexane-1,2-diamine
97%
- Product Code: 126734
Alias:
(1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)-1,2-cyclohexanediamine (1S,2S)-N,N'-1,2 -Cyclohexanediylbis[N-hydroxy-α-phenyl-phenylacetamide]
CAS:
1217464-22-6
| Molecular Weight: | 534.66 g./mol | Molecular Formula: | C₃₄H₃₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11044410 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its structure, featuring multiple functional groups, makes it effective in asymmetric synthesis, particularly in reactions that require high enantioselectivity. It is often employed in the formation of carbon-carbon or carbon-heteroatom bonds, aiding in the production of complex molecules with specific stereochemistry. Additionally, its ability to coordinate with metal ions enhances its use in metal-catalyzed reactions, contributing to the development of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and selectivity make it a valuable tool in advanced synthetic chemistry applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Light Yellow To Light Orange Powder To Crystal |
| Purity (%) | 95.0-96.5 |
| Specific Rotation [A]20/D(C=1, CHCl3) | -95.0 to -85.0 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | €150.11 |
+
-
|
(1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)cyclohexane-1,2-diamine
This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its structure, featuring multiple functional groups, makes it effective in asymmetric synthesis, particularly in reactions that require high enantioselectivity. It is often employed in the formation of carbon-carbon or carbon-heteroatom bonds, aiding in the production of complex molecules with specific stereochemistry. Additionally, its ability to coordinate with metal ions enhances its use in metal-catalyzed reactions, contributing to the development of pharmaceuticals, agrochemicals, and fine chemicals. Its stability and selectivity make it a valuable tool in advanced synthetic chemistry applications.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
€0.00
€0.00
Total :