98-22-6

Basic information

• Product Name: 2,6-DIBROMO-4-TERT-BUTYL-PHENOL
• Synonyms: 2,6-DIBROMO-4-TERT-BUTYL-PHENOL;4-tert-Butyl-2,6-dibromophenol;NSC 74538;Phenol, 2,6-dibroMo-4-(1,1-diMethylethyl)-
• CAS NO: 98-22-6
• Molecular Formula: C₁₀H₁₂Br₂O
• Molecular Weight: 308.01
• Mol File: 98-22-6.mol
• Article Data: 14

Chemical Properties

• Melting Point: 70-71℃
• Boiling Point: 256℃
• Flash Point: 108℃
• Appearance: /
• Density: 1.647
• Vapor Pressure: 0.0101mmHg at 25°C
• Refractive Index: 1.576
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2,6-DIBROMO-4-TERT-BUTYL-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIBROMO-4-TERT-BUTYL-PHENOL(98-22-6)
• EPA Substance Registry System: 2,6-DIBROMO-4-TERT-BUTYL-PHENOL(98-22-6)

Safety Data

• Hazardous Substances Data: 98-22-6(Hazardous Substances Data)

Usage

General Description

2,6-DIBROMO-4-TERT-BUTYL-PHENOL is a chemical compound commonly used as a biocide and preservative. It is a white crystalline solid with a phenolic odor and is soluble in organic solvents such as ethanol and acetone. This chemical is effective in inhibiting the growth of bacteria, fungi, and algae, making it useful in various industrial and agricultural applications. However, it is important to handle and use this compound with care as it is toxic if ingested, inhaled, or absorbed through the skin. Additionally, 2,6-DIBROMO-4-TERT-BUTYL-PHENOL is harmful to aquatic organisms and may cause long-term adverse effects in the environment.

InChI:InChI=1/C10H12Br2O/c1-10(2,3)6-4-7(11)9(13)8(12)5-6/h4-5,13H,1-3H3

Upstream product

• 7726-95-6 bromine 
• 98-54-4 para-tert-butylphenol 
• 90-15-3 α-naphthol 
• 110387-88-7 2,6-dibromo-4-nitro-4-tbutyl-2,5-cyclohexadien-1-one 

Downstream Products

• 61305-82-6 2,6-Dibrom-4-hydroxy-4-tert.-butyl-cyclohexa-2,5-dienon 
• 61306-36-3 2,6-Dibrom-4-methoxy-4-tert.-butylcyclohexa-2,5-dienon 
• 6766-84-3 4-(tert-butyl)-2,6-dimethoxyphenol 
• 1165739-43-4 1,3-dibromo-2-(3-bromopropoxy)-5-tert-butylbenzene 
• 1165738-71-5 1,3-dibromo-2-(2-bromoethoxy)-5-tert-butylbenzene 
• 171977-31-4 tetraphenylantimony 2,6-dibromo-4-tert-butylphenoxide 
• 61306-23-8 Butyric acid 3,5-dibromo-1-tert-butyl-4-oxo-cyclohexa-2,5-dienyl ester 
• 61306-28-3 Isobutyric acid 3,5-dibromo-1-tert-butyl-4-oxo-cyclohexa-2,5-dienyl ester 
• 61306-14-7 Propionic acid 3,5-dibromo-1-tert-butyl-4-oxo-cyclohexa-2,5-dienyl ester 
• 61306-19-2 Acetic acid 3,5-dibromo-1-tert-butyl-4-oxo-cyclohexa-2,5-dienyl ester 
• 94719-17-2 2-bromo-4-tert-butyl-6-triphenylsilylphenoxytrimethylsilane 
• 94719-15-0 2-trimethylsilyl-4-tert-butyl-6-triphenylsilylphenol 
• 85903-14-6 2-triethylsilyl-6-bromo-4-tert-butylphenoxytrimethylsilane 
• 85903-15-7 2-trimethylsilyl-4-tert-butyl-6-triethylsilylphenol 

Relevant articles and documents

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Selective Bromination of β-Positions of Porphyrin by Self-Catalytic Behaviour of VOTPP: Facile Synthesis, Electrochemical Redox Properties and Catalytic Application

Oxidovanadium(IV) complex of β-octabromo-meso-tetraphenylporphyrin, {[VIVO(TPPBr8)], 2} was synthesized by self-catalytic oxidative bromination of meso-tetraphenylporphyrinatooxidovanadium(IV) {[VIVO(TPP), 1} in excellent yield under mild conditions at 25 °C and its structure was confirmed by single crystal X-ray study. UV-Vis and 1H NMR spectra further confirmed that the meso-phenyl rings are not brominated and thus emphasizes on the selectivity as well as synthetic importance of this catalytic method. In the presence of substrates e. g. phenol derivatives, 1 biomimics the vanadium bromoperoxidase (VBPO) enzyme and catalyses the oxidative bromination of substrates in water at 25 °C. Remarkably, 2 also catalyses the oxidative bromination of phenol derivatives under similar reaction conditions with very high turnover frequency (TOF) values (ca. 29 s?1) along with its recyclability. It was found that 2 showed superior catalytic performance as compared to 1 because of its electron deficient nature due to electron withdrawing bromo substituents and robust saddle shaped nonplanar structure (further supported by DFT studies).

Microflow fluorinations of benzynes: Efficient synthesis of fluoroaromatic compounds

Fluorinated aromatic compounds are found in a variety of biologically active compounds, including clinical drugs and agrochemicals. Therefore, the synthesis of aryl fluorides is particularly important in the medicinal and process chemistry fields. In this

Binuclear complexes of Ni(i) from 4-terphenyldithiophenol

Binuclear complexes of Ni(i) have been prepared from a 4-terphenyldithiophenol ligand. Steric effects were found to determine the formation of coordination isomeric structures that differ in the nature of metal-to-ligand bonding. Coordination of spatially