(1S,2S)-(-)-1,2-Diaminocyclohexane D-tartrate
95%
- Product Code: 71593
Alias:
(1S,2S)-(-)-1,2-Cyclohexanediamine D-tartrate
CAS:
67333-70-4
Molecular Weight: | 264.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₆ |
---|---|---|---|
EC Number: | MDL Number: | MFCD00191980 | |
Melting Point: | 280-284 °C (dec.)(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
Used as a chiral resolving agent in the synthesis of optically active compounds, particularly in pharmaceuticals. It helps separate enantiomers, ensuring the production of single-isomer drugs with higher efficacy and fewer side effects.
Applied in asymmetric catalysis to create chiral intermediates for complex organic reactions. This is crucial in the production of fine chemicals and active pharmaceutical ingredients (APIs).
Employed in the preparation of chiral ligands for transition metal catalysts, enhancing stereoselectivity in chemical transformations.
Used in research and development for studying chiral molecules and their interactions, aiding in the design of new drugs and materials.
Also serves as a building block in organic synthesis, contributing to the creation of structurally diverse compounds with specific stereochemical properties.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White - Almost white - Pale-yellow Crystal - Powder |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿330.00 |
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5.000 | 10-20 days | ฿440.00 |
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25.000 | 10-20 days | ฿1,490.00 |
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100.000 | 10-20 days | ฿5,060.00 |
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(1S,2S)-(-)-1,2-Diaminocyclohexane D-tartrate
Used as a chiral resolving agent in the synthesis of optically active compounds, particularly in pharmaceuticals. It helps separate enantiomers, ensuring the production of single-isomer drugs with higher efficacy and fewer side effects.
Applied in asymmetric catalysis to create chiral intermediates for complex organic reactions. This is crucial in the production of fine chemicals and active pharmaceutical ingredients (APIs).
Employed in the preparation of chiral ligands for transition metal catalysts, enhancing stereoselectivity in chemical transformations.
Used in research and development for studying chiral molecules and their interactions, aiding in the design of new drugs and materials.
Also serves as a building block in organic synthesis, contributing to the creation of structurally diverse compounds with specific stereochemical properties.
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