5-Bromo-2-fluorotoluene

Suppliers

Names

[ Name ]:
5-Bromo-2-fluorotoluene

[Synonym ]:
4-Bromo-1-fluoro-2-methylbenzene
4-fluoro-3-methyl-1-bromo-benzene
Benzene,4-bromo-1-fluoro-2-methyl
1-bromo-4-fluoro-3-methylbenzene
5-Bromo-2-fluorotoluene
FR DE B1
5-BROMO-2-FLUORTOLUENE
5-Bromo-2-flurotoluene
2-FLUORO-5-BROMOTOLUENE
MFCD00000343
Benzene, 4-bromo-1-fluoro-2-methyl-
4-bromo-1-fluoro-2-methyl-benzene
EINECS 257-202-9

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
180.8±20.0 °C at 760 mmHg

[ Molecular Formula ]:
C₇H₆BrF

[ Molecular Weight ]:
189.025

[ Flash Point ]:
73.9±0.0 °C

[ Exact Mass ]:
187.963684

[ LogP ]:
3.44

[ Vapour Pressure ]:
1.2±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.527

[ Water Solubility ]:
INSOLUBLE

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29036990

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

4-(4-fluoro-3-methylphenyl)-4-oxobutanoic acid
(5-Bromo-2-fluorophenyl)methanol
2-Fluoro-5-bromobenzylbromide
4-Fluoro-3-methylbenzaldehyde
3-Methyl-4-fluorophenylboronic acid
4-Fluoro-3-methylbenzonitrile
5-Bromo-2-fluoro-3-methylbenzaldehyde

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Facilitated catecholamine transport through bulk and polymer-supported liquid membranes. Paugam M-F, et al.

J. Am. Chem. Soc. 118(41) , 9820-25, (1996)

Synthesis of 3-arylpropylamine derivatives from aryl halides using Heck reaction. Baek GH, et al.

Bull. Korean Chem. Soc. 20(2) , 233, (1999)

5-bromo-4-chloro-2-fluorotoluene
5-bromo-2-cyclopropyl-4-methoxy-6-(2-methylpropyl)pyrimidine
(5-bromo-2-hydroxy-3-methoxyphenyl)methyl-(2-methyl-1-phenylpropan-2-yl)azanium,chloride
5-bromo-2-ethylbenzaldehyde
5-bromo-2-pyridin-4-yl-1,3-benzoxazole
(5-bromo-2-hydroxy-3-methoxyphenyl)methyl-(2-phenylethyl)azanium,chloride
4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-({[1-(methoxymethyl)cyclobutyl]methyl}carbamoyl)butanoic acid
rac-(1R,2S)-2-(3-cyclopropylpropyl)cyclohexan-1-ol
(4S,4aR,5R,5aS,12aS)-4-(Dimethylamino)-11a-fluoro-1,4,4a,5,5a,6,11,11a,12,12a-decahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-2-naphthacenecarboxamide
4-(4-bromo-1-methyl-1H-pyrazol-5-yl)pyrrolidin-3-ol
2-(2,5-dihydro-1H-pyrrol-2-yl)-1-methylcyclohexan-1-ol
3-(dibenzylcarbamoyl)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid
3-ethoxy-4-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylbutanamido]butanoic acid
7-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methoxypropanamido]heptanoic acid
N-[7-[[3-O-(Aminocarbonyl)-6-deoxy-4-O-methyl-I+/--L-mannopyranosyl]oxy]-4-hydroxy-8-methyl-2-oxo-2H-1-benzopyran-3-yl]-4-hydroxy-3-(3-methyl-2-buten-1-yl)benzamide
5-(2-Methylbutan-2-yl)-1,2,3,6-tetrahydropyridin-3-ol

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