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

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

1,2,3-Benzenetriol, 5-broMo- Basic information
Application
Product Name:1,2,3-Benzenetriol, 5-broMo-
Synonyms: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;5-Bromo-1,2,3-benzenetriol;5-Bromobenzene-1,2,3-triol
CAS:16492-75-4
MF:C6H5BrO3
MW:205.01
EINECS:815-228-3
Product Categories:
Mol File:16492-75-4.mol
1,2,3-Benzenetriol, 5-broMo- Structure
1,2,3-Benzenetriol, 5-broMo- Chemical Properties
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. under inert gas (nitrogen or Argon) at 2–8 °C
form powder
pka8.32±0.15(Predicted)
color Dark fawn/beige
InChIInChI=1S/C6H5BrO3/c7-3-1-4(8)6(10)5(9)2-3/h1-2,8-10H
InChIKeyGZKWULQSPPFVMV-UHFFFAOYSA-N
SMILESC1(O)=CC(Br)=CC(O)=C1O
Safety Information
HS Code 2908190090
MSDS Information
1,2,3-Benzenetriol, 5-broMo- Usage And Synthesis
Application5-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.
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
1,2,3-Benzenetriol, 5-broMo- Preparation Products And Raw materials
Raw materials1-Bromo-3,4,5-trimethoxybenzene-->Dichloromethane-->Boron tribromide
Tag:1,2,3-Benzenetriol, 5-broMo-(16492-75-4) Related Product Information
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