(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
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
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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