CAS 2374-05-2: 4-Bromo-2,6-dimethylphenol
Formula:C8H9BrO
InChI:InChI=1S/C8H9BrO/c1-5-3-7(9)4-6(2)8(5)10/h3-4,10H,1-2H3
InChI key:InChIKey=ZLVFYUORUHNMBO-UHFFFAOYSA-N
SMILES:OC1=C(C)C=C(Br)C=C1C
Synonyms:- 2,6-Dimethyl-4-bromophenol
- 2,6-Xylenol, 4-bromo-
- 4-Bromo-2,6-xylenol
- NSC 63922
- Phenol, 4-bromo-2,6-dimethyl-
- 4-Bromo-2,6-dimethylphenol
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Found 8 products.
4-Bromo-2,6-dimethylphenol
CAS:Formula:C8H9BrOPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:201.06LABOTEST-BB LT03506639
CAS:Formula:C8H9BrOPurity:95%Color and Shape:SolidMolecular weight:201.060459999999984-Bromo-2,6-dimethylphenol
CAS:4-Bromo-2,6-dimethylphenolFormula:C8H9BrOPurity:98%Color and Shape: light red to very dark red/brown crystalline solidMolecular weight:201.06g/mol4-Bromo-2,6-dimethylphenol, 99%
CAS:It is used as a preservatives for coatings, slurries and to control microbial fouling in paper mills , oil field and leather process and water treatment process against microbial attack. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C8H9BrOPurity:99%Color and Shape:Cream or red to brown, Crystals or powder or crystalline powder or lumpy solidMolecular weight:201.064-Bromo-2,6-dimethylphenol
CAS:Purity:95.0%Color and Shape:Solid, Light brown powderMolecular weight:201.063003540039064-Bromo-2,6-dimethylphenol
CAS:4-Bromo-2,6-dimethylphenolFormula:C8H9BrOPurity:95+%Color and Shape: red/brown crystalline needlesMolecular weight:201.06g/mol4-Bromo-2,6-dimethylphenol
CAS:4-Bromo-2,6-dimethylphenol is a copolymerization product of bromophenols. It has been shown to be effective in the Suzuki coupling reaction with 4-(chloromethyl)benzeneboronic acid and n-butyllithium as the catalyst. The mechanism of this reaction is initiated by nucleophilic substitution of the chlorine atom in 4-bromo-2,6-dimethylphenol for the carbonyl group in 4-(chloromethyl)benzeneboronic acid. The chloride ion then leaves and combines with hydrogen sulfate, forming hydrochloric acid with a pH of 0.5 to 1.0, which can be used as a reaction medium for polymerization and depolymerization reactions such as gel permeation chromatography. This process is called ion exchange polymerization or ion exchange depolymerization.Purity:Min. 95%
