ChemicalBook--->CAS DataBase List--->636-32-8

636-32-8

636-32-8 Structure

636-32-8 Structure
IdentificationBack Directory
[Name]

1,2,4,5-tetrahydroxybenzene
[CAS]

636-32-8
[Synonyms]

1,2,4,5-Benzenetetrol
benzene-1,2,4,5-tetrol
Benzene-1,2,4,5-tetraol
1,2,4,5-tetrahydroxybenzene
benzene-1,2,4,5-tetrol,≥98%
Phloroglucinol Impurity 206
5-Hydroxybenzene-1,2,4-triol
[Molecular Formula]

C6H6O4
[MOL File]

636-32-8.mol
[Molecular Weight]

142.11
Chemical PropertiesBack Directory
[Melting point ]

210 °C
[Boiling point ]

477.1±40.0 °C(Predicted)
[density ]

1.709±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

9.72±0.23(Predicted)
[Appearance]

Gray to brown Solid
[CAS DataBase Reference]

636-32-8
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

1,2,4,5-tetrahydroxybenzene(636-32-8)1HNMR
1,2,4,5-tetrahydroxybenzene(636-32-8)ESR
Hazard InformationBack Directory
[Synthesis]

2,5-DIHYDROXY-1,4-BENZOQUINONE

615-94-1

1,2,4,5-tetrahydroxybenzene

636-32-8

General procedure for the synthesis of 1,2,4,5-benzenetetrol from 2,5-dihydroxy-1,4-benzoquinone: To a solution of 2,5-dihydroxy-1,4-benzoquinone (2.0 g, 1.0 eq.) in hydrochloric acid (110 mL) was slowly added tin particles (2.068 g, 1.2 eq.). The reaction mixture was heated to 110 °C and maintained for 1 hour. When the temperature of the reaction solution was reduced to 50-60 °C, thermal filtration was carried out and the filtrate was subsequently cooled to 0 °C to promote crystallization, resulting in colorless crystals of 1,2,4,5-benzenetetrol (1.450 g, 74%). The product was characterized by 1H NMR (MeOD, 300 MHz): δ 5.0 (broad peak, 4H), 5.90 (single peak, 2H).ESI-MS showed molecular ion peak m/z 145.03 [M+].

[References]

[1] Journal of Organometallic Chemistry, 2000, vol. 614-615, p. 188 - 194
[2] Journal of Organic Chemistry, 2008, vol. 73, # 12, p. 4452 - 4457
[3] Chemistry - A European Journal, 2013, vol. 19, # 51, p. 17349 - 17357
[4] European Journal of Medicinal Chemistry, 2013, vol. 67, p. 269 - 279
[5] Collection of Czechoslovak Chemical Communications, 2012, vol. 77, # 3, p. 201 - 209
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