ChemicalBook--->CAS DataBase List--->16492-75-4

16492-75-4

16492-75-4 Structure

16492-75-4 Structure
IdentificationBack Directory
[Name]

1,2,3-Benzenetriol, 5-broMo-
[CAS]

16492-75-4
[Synonyms]

5-Bromobenzene-1,2,3-triol
1,2,3-Benzenetriol, 5-broMo-
1-Bromo-(3,4,5-trihydroxy)benzene
5-bromo-(1,2,3-trihydroxy)benzene
1,2,3-Benzenetriol, 5-broMo- ISO 9001:2015 REACH
[EINECS(EC#)]

815-228-3
[Molecular Formula]

C6H5BrO3
[MDL Number]

MFCD22555992
[MOL File]

16492-75-4.mol
[Molecular Weight]

205.01
Chemical PropertiesBack Directory
[Melting point ]

118 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
[Boiling point ]

345.9±37.0 °C(Predicted)
[density ]

2.031±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

powder
[pka]

8.32±0.15(Predicted)
[color ]

Dark fawn/beige
[InChI]

InChI=1S/C6H5BrO3/c7-3-1-4(8)6(10)5(9)2-3/h1-2,8-10H
[InChIKey]

GZKWULQSPPFVMV-UHFFFAOYSA-N
[SMILES]

C1(O)=CC(Br)=CC(O)=C1O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H332-H319-H335
[Precautionary statements ]

P260-P280-P312
[HS Code ]

2908190090
Questions And AnswerBack Directory
[Application]

5-Bromo-1,2,3-benzenepyrogallol can be used as an organic synthesis intermediate and a pharmaceutical intermediate, mainly in laboratory research and development processes and chemical production processes.
Spectrum DetailBack Directory
[Spectrum Detail]

1,2,3-Benzenetriol, 5-broMo-(16492-75-4)1HNMR
1,2,3-Benzenetriol, 5-broMo-(16492-75-4)FT-IR
Hazard InformationBack Directory
[Synthesis]

1-Bromo-3,4,5-trimethoxybenzene

2675-79-8

1,2,3-Benzenetriol, 5-broMo-

16492-75-4

General procedure for the synthesis of 5-bromo-1,2,3-benzenetriol from 1-bromo-3,4,5-trimethoxybenzene: 7.44 g (30.24 mmol) of 3,4,5-trimethoxy-1-bromobenzene and 70 mL of anhydrous methylene chloride were added to a four-necked flask and the mixture was cooled to -78 °C. Subsequently, 325.0 g (99.8 mmol) of boron tribromide (BBr3) was slowly added dropwise, and after completion of the dropwise addition, the reaction mixture was continued to be stirred at -78 °C for 1 hour. Upon completion of the reaction, the mixture was slowly warmed to room temperature and carefully poured into 200 mL of ice water to precipitate the product. The precipitate was collected by filtration to give 6.8 g (quantitative yield) of 5-bromo-1,2,3-benzenetriol as a white powder. The m/z of 5-bromo-1,2,3-benzenetriol was analyzed by mass spectrometry to be 206.01 ([M + H]+).

[References]

[1] Journal of Polymer Science, Part A: Polymer Chemistry, 2012, vol. 50, # 6, p. 1187 - 1196
[2] Angewandte Chemie - International Edition, 2017, vol. 56, # 18, p. 5031 - 5034
[3] Angew. Chem., 2017, vol. 129, # 18, p. 5113 - 5116,4
[4] Patent: JP6236813, 2017, B2. Location in patent: Paragraph 0184; 0185
[5] Journal of the American Chemical Society, 2011, vol. 133, # 34, p. 13437 - 13444
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