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CAS No. : | 3102-87-2 | MDL No. : | MFCD00007905 |
Formula : | C10H16N2 | Boiling Point : | - |
Linear Structure Formula : | (CH3)4C6(NH2)2 | InChI Key : | WCZNKVPCIFMXEQ-UHFFFAOYSA-N |
M.W : | 164.25 | Pubchem ID : | 76548 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
62% | In ethanol; for 3h;Reflux; | L1 was synthesized using a modified literatureprocedure.10-13 An ethanolic solution (15 mL) of3,5-diiodine-2-hydroxybenzaldehyde (1.244 g, 2 mmol)was added dropwise to an ethanolic solution (15 mL) of2,3,5,6-tetramethylphenylenediamine (0.164 g, 1 mmol).The reaction mixture was refluxed for 3 h and then stirredovernight at room temperature. Subsequently, the resultingyellow solution was cooled, affording a yellow precipitate,which was filtered off and washed with hexane. Yield:62%; mp > 300 C; elemental analysis for C24H20N2O2I4(anal. calcd. (found)): C, 32.89 (32.70); H, 2.28 (2.45),N: 3.19 (3.30); IR (KBr, ± 4 cm-1) υ / cm-1 3433 (O-H),2916 (C-H, aromatic), 1617 (C=N, imine), 1545 and1432 (C=C, aromatic), 1277 (C-N), 1155 and 1064(C-O, phenol), 645 (C-I); 1H NMR (300 MHz, CDCl3,25 C) δ 8.23 (s, 2H, CH=N), 7.24-7.05 (m, 4H, ArH),2.35 (s, 12H, CH3). |
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