3354-82-3

Usage

Uses

Used in Organic Synthesis:
1,3,5-Benzenetriol, 2,4,6-tribromo(9CI) is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions. Its presence enhances the reactivity and selectivity of the synthesis process, making it a valuable component in the production of complex organic molecules.
Used in Flame Retardants Production:
In the flame retardants industry, 1,3,5-Benzenetriol, 2,4,6-tribromo(9CI) is used as a precursor for the development of effective flame retardant compounds. Its bromine content contributes to the fire-resistant properties of the final products, making it an essential component in the creation of safer materials.
Used in Pharmaceutical Manufacturing:
1,3,5-Benzenetriol, 2,4,6-tribromo(9CI) plays a role in the pharmaceutical industry as a precursor for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Industrial Product Development:
This chemical compound is also utilized in the manufacturing of various industrial products due to its versatile properties. Its presence can enhance the performance and characteristics of a wide range of products, making it a valuable asset in the chemical industry.

InChI:InChI=1/C6H3Br3O3/c7-1-4(10)2(8)6(12)3(9)5(1)11/h10-12H

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 64-17-5 ethanol 
• 67-66-3 chloroform 
• 2161-86-6 2,4-diacetylphloroglucinol 
• 2161-87-7 1,3,5-triacetyl-2,4,6-trihydroxybenzene 
• 95412-48-9 6,8-dibromoquercetin 
• 7726-95-6 bromine 
• 480-15-9 datiscetin 
• 64-19-7 acetic acid 
• 7732-18-5 water 
• 60-29-7 diethyl ether 
• 83-30-7 acide 2,4,6-trihydroxybenzoique 
• 3770-80-7 2,4,6-trimethoxybenzophenone 
• 861538-72-9 2,4,6-triacetyl-cyclohexane-1,3,5-trione 

Downstream Products

• 108-73-6 3,5-dihydroxyphenol 
• 84743-75-9 2,4-dibromo-1,3,5-trihydroxybenzene 
• 84743-77-1 2-bromo-1,3,5-trihydroxybenzene 
• 741700-85-6 C₃₃H₁₂Br₃F₉O₉ 
• 96820-10-9 2-bromophloroglucinol triacetate 
• 217825-79-1 tribromophloroglucinol triacrylate 
• 504-02-9 1,3-cylohexanedione 
• 108-46-3 recorcinol 

Relevant academic research and scientific papers

NANOSHEET AND METHOD FOR MANUFACTURING THE SAME

Provided are a nanosheet and a manufacturing method thereof. The nanosheet comprises a compound of Formula 1. Chemical Formula 1. A manufacturing method of the nanosheet is as follows. The step of halogenating the phloroglucinol to form trihalogenic phloroglucinol and reacting the trihalogentle phloroglucinol with nucleophilic substitution.

Method of making chlorofluoroethers

A method is provided for preparation of chlorofluoroethers ClCF2CFClOR8f and Cl2CFCFClOR8f by direct fluorination of Cl2CHCH2OR8 and Cl3CCH2OR8, respectively, wherein R8 is a C1-C20 alkyl-or acyl-containing group optionally up to 5 ether oxygen atoms and optionally substituted by functional groups and R81, is the corresponding perfluoroalkyl or perfluoracyl-containing group.

Bromophloroglucinols and their methyl ethers

All 16 bromination products of phloroglucinol and its methyl ethers, as well as five bromoresorcinols and three of their dimethyl ethers, were synthesized and analyzed by nuclear magnetic resonance spectroscopy.Two or three equivalents of bromine convert phloroglucinol to di- and tribromophloroglucinol, 5-methoxyresorcinol to the tri- and 2,4-dibromo, 3,5-dimethoxyphenol to the tri- and 2,6-dibromo, and 1,3,5-trimethoxybenzene to the dibromo compound.With one equivalent of bromine, 3,5-dimethoxyphenol reacts preferentially at C-2 while 5-methoxyresorcinol gives both monobromo isomers.Partial debromination with sodium sulfite yields successively 2,4-dibromo- and 2-bromo-5-methoxyresorcinol from the tribromo compound but fails with brominated 3,5-dimethoxyphenol.In the resorcinol series, C-2 is invariably the least reactive position. 4,6-Dibromo-5-methoxyresorcinol and 2,4-dibromo-3,5-dimethoxyphenol are accessible by methylation of dibromophloroglucinol, obtained from 3,5-dibromo-2,4,6-trihydroxybenzoic acid by decarboxylation.In contrast to resorcinol and tribromoresorcinol, the partial bromination of pholoroglucinol and debromination of tribromopholoroglucinol are not selective.The 13Cnmr spectra of bromophloroglucinol methyl ethers show characteristic downfield shifts for methoxy groups orthogonal to the aromatic ring plane.

Bromination of Phenols by Use of Benzyltrimethylammonium Tribromide

The reaction of phenols with benzyltrimethylammonium tribromide in dichloromethane-methanol for 1 h at room temperature gave polybromophenols in good yields.