(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine
98.0%
- Product Code: 70784
CAS:
138517-66-5
Molecular Weight: | 236.31 g./mol | Molecular Formula: | C₁₆H₁₆N₂ |
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EC Number: | MDL Number: | MFCD06654768 | |
Melting Point: | 158 °C | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its unique structure, featuring a fused ring system with amine groups, makes it valuable for constructing chiral compounds, particularly in asymmetric synthesis. It is often employed in the development of pharmaceuticals, where its stereochemistry can influence the biological activity of the final drug product. Additionally, it finds use in materials science for creating specialized polymers or ligands that require precise spatial arrangements. Its role in catalysis is also notable, as it can act as a precursor for chiral catalysts used in enantioselective reactions.
Product Specification:
Test | Specification |
---|---|
Melting point | 156 160? |
PURITYHPLC | 98 100% |
PURITYNONAQUEOUS TITRATION | 98 100% |
A20DC1METHANOL | 17 22 |
INFRARED SPECTROMETRY | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,382.00 |
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0.250 | 10-20 days | ฿13,860.00 |
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(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its unique structure, featuring a fused ring system with amine groups, makes it valuable for constructing chiral compounds, particularly in asymmetric synthesis. It is often employed in the development of pharmaceuticals, where its stereochemistry can influence the biological activity of the final drug product. Additionally, it finds use in materials science for creating specialized polymers or ligands that require precise spatial arrangements. Its role in catalysis is also notable, as it can act as a precursor for chiral catalysts used in enantioselective reactions.
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