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Product Name:(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diaMine CAS:138517-66-5 Purity:98.0%(LC&T) Package:100MG,1G
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Product Name:(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diaMine CAS:138517-66-5 Purity:>98.0%(LC)(T) Package:100Mg;1g Remarks:D3445
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Product Name:(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine CAS:138517-66-5 Purity:98.0% LC&T Package:100MG,1G
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| (11S,12S)-9,10-DIHYDRO-9,10-ETHANOANTHRACENE-11,12-DIAMINE Basic information |
Product Name: | (11S,12S)-9,10-DIHYDRO-9,10-ETHANOANTHRACENE-11,12-DIAMINE | Synonyms: | (11S,12S)-9,10-DIHYDRO-9,10-ETHANOANTHRACENE-11,12-DIAMINE;(S,S)-11,12-Diamino-9,10-dihydro-9,10-ethanoanthracene;(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine >=95.0% (HPLC);(11S,12S)-11,12-diamino-9,10-dihydro-9,10-ethanoanthracene (R)-mandelate monoammonium salt;(11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine>9,10-Ethanoanthracene-11,12-diamine, 9,10-dihydro-, (11S,12S)- | CAS: | 138517-66-5 | MF: | C16H16N2 | MW: | 236.31 | EINECS: | | Product Categories: | Asymmetric Synthesis;Synthetic Organic Chemistry | Mol File: | 138517-66-5.mol | |
| (11S,12S)-9,10-DIHYDRO-9,10-ETHANOANTHRACENE-11,12-DIAMINE Chemical Properties |
Melting point | 158 °C | Boiling point | 396.7±42.0 °C(Predicted) | density | 1.195±0.06 g/cm3(Predicted) | refractive index | 20 ° (C=1, MeOH) | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | form | powder to crystal | pka | 9.38±0.40(Predicted) | color | White to Orange to Green | BRN | 8693351 |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26 | WGK Germany | 3 | HS Code | 2921.51.5000 |
| (11S,12S)-9,10-DIHYDRO-9,10-ETHANOANTHRACENE-11,12-DIAMINE Usage And Synthesis |
Uses | (11S,12S)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine is a chiral diamine, which can be used as a reactant:
- To synthesize pyridine based C2-symmetrical chiral organocatalysts via palladium catalyzed coupling reaction with 2-bromo-4-(alkylamino)pyridine.
- To prepare porous organic imine cages by cycloimination reaction with triformylbenzene.
- To synthesize Ga/Yb-Schiff base complex, which is utilized as a catalyst for the asymmetric synthesis of 5-amino-2-(hydroxyalkyl)oxazoles by enantioselective α-addition of α-isocyano amides to aldehydes.
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| (11S,12S)-9,10-DIHYDRO-9,10-ETHANOANTHRACENE-11,12-DIAMINE Preparation Products And Raw materials |
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