ChemicalBook--->CAS DataBase List--->7766-23-6

7766-23-6

7766-23-6 Structure

7766-23-6 Structure
IdentificationBack Directory
[Name]

3-BROMO-2-METHYLPHENOL
[CAS]

7766-23-6
[Synonyms]

3-BROMO-2-METHYLPHENOL
2-Methyl-3-broMophenol
Phenol, 3-bromo-2-methyl-
2-Bromo-6-hydroxytoluene, 3-Bromo-o-cresol
[Molecular Formula]

C7H7BrO
[MDL Number]

MFCD11100990
[MOL File]

7766-23-6.mol
[Molecular Weight]

187.03
Chemical PropertiesBack Directory
[Melting point ]

95°C
[Boiling point ]

220.79°C (rough estimate)
[density ]

1.3839 (rough estimate)
[refractive index ]

1.5772 (estimate)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

9.35±0.10(Predicted)
[color ]

Off-White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2908190090
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-2-METHYLPHENOL(7766-23-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Bromo-2-methylaniline

55289-36-6

3-BROMO-2-METHYLPHENOL

7766-23-6

General procedure for the synthesis of 3-bromo-2-methylphenol from 3-bromo-2-methylaniline: a solution of sodium was slowly added to a solution of 3-bromo-2-methylaniline (6 g, 32.2 mmol) in sulfuric acid (38.7 mL, 38.7 mmol) at 0 °C. The reaction mixture was stirred at 0°C for 15 minutes before sulfuric acid (13.75 mL, 258 mmol) was added, followed by warming the reaction system to 100°C and heating for 1 hour. After completion of the reaction, the mixture was diluted with water and extracted with ether (Et2O). The organic phase was dried and concentrated and purified by silica gel column chromatography to afford the target product 3-bromo-2-methylphenol (light brown solid, 4.92 g, 82% yield).

[References]

[1] Chemical Communications, 2003, # 10, p. 1170 - 1171
[2] Patent: US2011/82165, 2011, A1. Location in patent: Page/Page column 46
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 4, p. 1417 - 1431
[4] European Journal of Organic Chemistry, 2018, vol. 2018, # 17, p. 2013 - 2021
[5] Patent: US6831106, 2004, B1. Location in patent: Page column 19
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