3-Amino-1,2-benzenediol

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3-Amino-1,2-benzenediol Basic information
Product Name:3-Amino-1,2-benzenediol
Synonyms:3-Amino-1,2-benzenediol;1,2-Benzenediol, 3-aMino-;3-Amino benzene-1,2-diol / 3-Amino catechol hydrochloride;3-aMinobenzene-1,2-diol
CAS:20734-66-1
MF:C6H7NO2
MW:125.13
EINECS:
Product Categories:
Mol File:20734-66-1.mol
3-Amino-1,2-benzenediol Structure
3-Amino-1,2-benzenediol Chemical Properties
Melting point 142-145 °C
Boiling point 297.0±25.0 °C(Predicted)
density 1.412±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMF: 5 mg/ml; DMSO: 5 mg/ml; Ethanol: 10 mg/ml; PBS (pH 7.2): 1 mg/ml
form A solid
pka9.59±0.10(Predicted)
Safety Information
HazardClass IRRITANT
HS Code 2908190090
MSDS Information
3-Amino-1,2-benzenediol Usage And Synthesis
UsesDegradation of Acid Black 1 reveals the formation of 3-Aminocatechol as one of the intermediates.
Synthesis
2,3-DIMETHOXYANILINE

6299-67-8

3-Amino-1,2-benzenediol

20734-66-1

2,3-Dimethoxyaniline (438 μL, 3.26 mmol) was used as raw material and dissolved in dichloromethane (5.0 mL). A 1 mol/L solution of boron tribromide/dichloromethane (11.4 mL, 11.4 mmol) was slowly added dropwise at -78 °C under argon protection. After the dropwise addition, the reaction system was slowly warmed to room temperature and stirred overnight. Upon completion of the reaction, the reaction was quenched with saturated aqueous sodium bicarbonate solution and subsequently neutralized with saturated aqueous ammonium chloride solution. The reaction mixture was extracted with ethyl acetate and the organic phase was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford the target product 3-aminobenzene-1,2-diol (67 mg, 16% yield).

IC 50MMP-2: 20 μM (IC50); MMP-8: 26 μM (IC50); MMP-9: 16 μM (IC50); MMP-14: 16.3 μM (IC50)
References[1] Patent: JP2016/124812, 2016, A. Location in patent: Paragraph 0098
[2] Patent: US2003/65018, 2003, A1
[3] Patent: WO2007/71434, 2007, A1. Location in patent: Page/Page column 60-61
3-Amino-1,2-benzenediol Preparation Products And Raw materials
Raw materials2,3-Dimethoxyaniline-->Boron tribromide-->Dichloromethane
Preparation Products8-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one
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