3-Bromoanisole Chemical Properties

Melting point:

2 °C

Boiling point:

210-211 °C(lit.)

Density 

1.490 g/mL at 20 °C

vapor pressure 

38.39Pa at 25℃

refractive index 

n20/D 1.563(lit.)

Flash point:

200 °F

storage temp. 

Sealed in dry,Room Temperature

solubility 

DMSO (Sparingly), Methanol (Slightly)

form 

Liquid

Specific Gravity

1.477

color 

Clear colorless to slightly yellow-brown

PH

5.5 (H2O, 20℃)

Water Solubility 

Miscible in methanol, benzene, hexane, toluene and dichloromethane. Practically insoluble in water.

BRN 

1524687

Stability:

Stable. Combustible. Incompatible with strong oxidising agents, strong acids reducing agents.

InChIKey

PLDWAJLZAAHOGG-UHFFFAOYSA-N

LogP

3.03

CAS DataBase Reference

2398-37-0(CAS DataBase Reference)

NIST Chemistry Reference

Benzene, 1-bromo-3-methoxy-(2398-37-0)

EPA Substance Registry System

m-Bromoanisole (2398-37-0)

Safety Information

Hazard Codes 

Xi

Safety Statements 

23-24/25

WGK Germany 

3

F 

8

Hazard Note 

Irritant

TSCA 

T

HS Code 

29093038

MSDS

• Language:English Provider:1-Bromo-3-methoxybenzene
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

3-Bromoanisole Usage And Synthesis

Chemical Properties

3-Bromoanisole, also known as m-Bromoanisole, is a clear colorless to pale yellow oily liquid. The boiling point is 210-211°C (100kPa), 105°C (2.13kPa), the relative density is 1.477, the refractive index is 1.5635, and the flash point is 93°C. It is soluble in alcohol, ether, benzene, and carbon disulfide, but insoluble in water. It is commonly used as a raw material for organic synthesis.

Uses

3-Bromoanisole used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemicals.

Preparation

3-Bromoanisole is synthesized through a reaction between m-bromophenol and dimethyl sulfate. The synthesis method involves the following steps:
Dissolve m-bromophenol in a sodium hydroxide solution.
Slowly add dimethyl sulfate dropwise to the solution while stirring.
Heat the mixture and allow it to react for 1 hour.
Cool the reaction mixture to separate the colorless oil formed.
Extract the water layer with ether.
Dry the ether extract and then distill it to recover the ether.
Distill the residue obtained after recovering the ether, along with the colorless oil, under reduced pressure.
This distillation process results in the production of m-bromoanisole as the final product.
The overall yield of m-bromoanisole achieved through this process is 90%.

References

Application of Anisole, 2-Bromoanisole and 3-Bromoanisole as Overcharge Protection Additives in Lithium-Ion Batteries DOI:10.6023/A12110964
S. Ramalingam; S. Periandy. Spectroscopic investigation, computed IR intensity, Raman activity and vibrational frequency analysis on 3-bromoanisole using HF and DFT (LSDA/MPW1PW91) calculations. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2011, 78 (2), 835-843. DOI:10.1016/j.saa.2010.12.043
Bobby Glover; Kimberly A. Harvey; Bing Liu; Matthew J. Sharp; and Maria F. Tymoschenko. Regioselective Palladium-Catalyzed Arylation of 3-Carboalkoxy Furan and Thiophene. Org. Lett. 2003, 5 (3), 301-304. DOI:10.1021/ol027266q

3-Bromoanisole(2398-37-0)Related Product Information

• 1,2-Dibromobenzene
• 1,3-Dibromobenzene
• 2-Bromobenzonitrile
• 3-Bromobenzonitrile
• 3-Bromofluorobenzene
• 3-(Trifluoromethoxy)bromobenzene
• 3-Bromobenzyl alcohol
• 3-Nitrobenzyl bromide
• (3-NITROPHENYL)ACETIC ACID METHYL ESTER
• 3-Nitroacetophenone
• 3-Bromobenzyl bromide
• 3-Nitrobenzaldehyde
• 1-Bromo-3-iodobenzene
• 3-Bromobenzaldehyde
• 3-Bromobenzoic acid
• Bromine
• 2-BROMO-4,5-METHYLENEDIOXYCINNAMIC ACID
• 1-Bromo-3,4,5-trimethoxybenzene