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2,3-Diaminophenol

ALDRICH/340618 - 97%

CAS Number: 59649-56-8
Empirical Formula (Hill Notation): C6H8N2O
Molecular Weight: 124.14
MDL Number: MFCD00075199
Linear Formula: (H2N)2C6H3OH
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-340618-5G 5 g
 $174.00
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 340618-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 340618-5G

 

assay 97%
InChI 1S/C6H8N2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H,7-8H2
InChI key PCAXITAPTVOLGL-UHFFFAOYSA-N
mp 161-165 °C (lit.)
SMILES string Nc1cccc(O)c1N
Application: 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.
Packaging: 1, 5, 25 g in glass bottle
Purity 97%
mp 161-165 °C (lit.)
UNSPSC 12352100

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