2,3-Diaminophenol
2,3-Diaminophenol structure
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Common Name | 2,3-Diaminophenol | ||
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| CAS Number | 59649-56-8 | Molecular Weight | 124.141 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 303.6±27.0 °C at 760 mmHg | |
| Molecular Formula | C6H8N2O | Melting Point | 161-165 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 137.4±23.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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1,5-Benzoxazepines vs 1,5-benzodiazepines. one-pot microwave-assisted synthesis and evaluation for antioxidant activity and lipid peroxidation inhibition.
J. Med. Chem. 53(23) , 8409-20, (2010) Amino-1,5-benzoxazepines 2 and 5 and hydroxyl-1,5-benzodiazepines 3 and 6 have been synthesized in one-pot solvent-free conditions from 2,3-diaminophenol and ketones through microwave assisted acid catalysis, the benzoxazepine/benzodiazepine ratio depending o... |
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Pd(II) and Pt(II) complexes with aromatic diamines: study of their interaction with DNA.
J. Inorg. Biochem. 98(3) , 510-21, (2004) Pd(II) and Pt(II) new complexes with simple aromatic diamines were synthesised and characterised with the aim of studying their possible antitumour activity. The aromatic diamines chosen were 2,3-diaminotoluene (2,3 dat), 3,4-diaminotoluene (3,4 dat), 4,5-dia... |
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On benzo[b][1,4]diazepinium-olates, -thiolates and -carboxylates as anti-Hückel mesomeric betaines.
Org. Biomol. Chem. 1(23) , 4342-50, (2003) 2,3-Diaminophenol 4, 3,4-diaminophenol 5, 4-methoxy-1,2-diaminobenzene 6, 3,4-diaminobenzenethiol 7, 2,3-diaminobenzoic acid 8, and 3,4-diaminobenzoic acid 9 were reacted with 2,4-pentanedione to yield the corresponding benzo[b][1,4]diazepinium salts, respect... |
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Transition Met. Chem. (London) 31 , 169, (2006)
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Unsymmetrical tetradentate Schiff base complexes derived from 2, 3-diaminophenol and salicylaldehyde or 5-bromosalicylaldehyde. Ourari A, et al.
Transit. Met. Chem. 31(2) , 169-175, (2006)
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Electropolymerization of 2, 3-diaminophenol. Del Valle MA, et al.
J. Polym. Sci. A Polym. Chem. 38(9) , 1698-1703, (2000)
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