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| 2,3-Diaminophenol Basic information |
Product Name: | 2,3-Diaminophenol | Synonyms: | 2,3-DIAMINOPHENOL;2,3-Diaminophenolsulfate;2,3-Diaminophenol,97%;Phenol, 2,3-diaMino-;2,3-DiaMinophenol 97%;2,3-diaminophenol59649-56-8;1,2,3,4,5-Cyclopentanepentayl,1-[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-2-[(R)-(dimethylamino)phenylmethyl]-,ironsalt(2:6) | CAS: | 59649-56-8 | MF: | C6H8N2O | MW: | 124.14 | EINECS: | | Product Categories: | Organic Building Blocks;Oxygen Compounds;Phenol&Thiophenol&Mercaptan;Phenoles and thiophenoles;Phenols | Mol File: | 59649-56-8.mol | |
| 2,3-Diaminophenol Chemical Properties |
Melting point | 161-165 °C (lit.) | Boiling point | 303.6±27.0 °C(Predicted) | density | 1.343±0.06 g/cm3(Predicted) | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | pka | 9.81±0.10(Predicted) | form | Granular or Crystalline Powder or Crystals | color | White | CAS DataBase Reference | 59649-56-8(CAS DataBase Reference) |
Hazard Codes | Xn | Risk Statements | 20/22-36/37/38 | Safety Statements | 26 | RIDADR | UN 3259 8/PG 2 | WGK Germany | 3 | HS Code | 29222990 |
| 2,3-Diaminophenol Usage And Synthesis |
Chemical Properties | White to beige crystalline powder | Uses | 2,3-Diaminophenol was used:
- in one-pot microwave assisted synthesis of amino-1,5-benzoxazepines and hydroxyl-1,5-benzodiazepines
- in the electrosynthesis of poly(2,3-diaminophenol) via electro-oxidation
- in a synthesis of tetradentate Schiff base complexes via reaction with salicylaldehyde or 5-bromosalicylaldehyde and metals such as Mn(III), Ni(II) and Cu(II)
| General Description | 2,3-Diaminophenol is an aromatic diamine and forms Pd(II) and Pt(II) complexes. 2,3-Diaminophenol reacts with 2,4-pentanedione to yield the corresponding benzo[b][1,4]diazepinium salts. 2,3-Diaminophenol reacts with salicylaldehyde or 5-bromosalicylaldehyde in absolute ethanol to yield new unsymmetrical Schiff base. |
| 2,3-Diaminophenol Preparation Products And Raw materials |
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