trans-1,2-Cyclohexanediamine
98%
- Product Code: 72998
Alias:
trans-1,2-cyclohexanediamine; (±)-trans-1,2-diaminocyclohexane
CAS:
1121-22-8
| Molecular Weight: | 114.19 g./mol | Molecular Formula: | C₆H₁₄N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00063747 | |
| Melting Point: | 14-15 °C(lit.) | Boiling Point: | 79-81 °C15 mm Hg(lit.) |
| Density: | 0.951 g/mL at 25 °C(lit.) | Storage Condition: | 2~8℃ |
Product Description:
Trans-1,2-cyclohexanediamine is widely used as a chiral ligand in asymmetric synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its ability to induce enantioselectivity makes it valuable in catalytic reactions, such as hydrogenation and oxidation, where it helps create specific stereoisomers of compounds. This chemical is also employed in the synthesis of metal complexes, which are used as catalysts in organic transformations. Additionally, it serves as a building block in the preparation of polymers and resins, contributing to their structural properties. In the field of coordination chemistry, it is utilized to develop ligands for metal ions, aiding in the study of catalytic processes and material science. Its versatility and effectiveness in controlling stereochemistry make it a key component in advanced chemical research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 98-100 |
| REFRACTIVE INDEX N20D | 1.487-1.4905 |
| APPEARANCE | Colorless to light yellow liquid |
| INFRARED SPECTRUM | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 2.000 | 10-20 days | $16.07 |
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| 10.000 | 10-20 days | $44.70 |
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| 50.000 | 10-20 days | $160.72 |
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| 250.000 | 10-20 days | $611.75 |
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trans-1,2-Cyclohexanediamine
Trans-1,2-cyclohexanediamine is widely used as a chiral ligand in asymmetric synthesis, particularly in the production of pharmaceuticals and fine chemicals. Its ability to induce enantioselectivity makes it valuable in catalytic reactions, such as hydrogenation and oxidation, where it helps create specific stereoisomers of compounds. This chemical is also employed in the synthesis of metal complexes, which are used as catalysts in organic transformations. Additionally, it serves as a building block in the preparation of polymers and resins, contributing to their structural properties. In the field of coordination chemistry, it is utilized to develop ligands for metal ions, aiding in the study of catalytic processes and material science. Its versatility and effectiveness in controlling stereochemistry make it a key component in advanced chemical research and industrial applications.
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