ChemicalBook > Product Catalog > Organic Chemistry > Ethers and derivatives > Ethers, ether-alcohols, ether phenol derivatives > 2-Bromo-5-methoxytoluene
2-Bromo-5-methoxytoluene
2-Bromo-5-methoxytoluene Basic information
- Product Name:
- 2-Bromo-5-methoxytoluene
- Synonyms:
-
- 2-Bromo-5-methoxytoluene, 1-Bromo-4-methoxy-2-methylbenzene, 4-Bromo-3-methylphenyl methyl ether
- 2-BroMo-5-Methoxytoluene (BMA)
- 4-BroMo-3-Methylanisole, 97%, 97%
- 2-Bromo-4-methoxy-1-methylbenzene
- 1-BROMO-4-METHOXY-2-METHYLBENZENE
- 2-BROMO-5-METHOXYTOLUENE
- 2-(3-bromophenyl)-2-methoxyacetic acid
- 3-Methyl-4-bromoanisole
- CAS:
- 27060-75-9
- MF:
- C8H9BrO
- MW:
- 201.06
- Product Categories:
-
- Halogen toluene
- Anisoles, Alkyloxy Compounds & Phenylacetates
- Aromatic Hydrocarbons (substituted) & Derivatives
- Bromine Compounds
- Mol File:
- 27060-75-9.mol
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2-Bromo-5-methoxytoluene Chemical Properties
- Melting point:
- 16.5 °C
- Boiling point:
- 111-112 °C15 mm Hg(lit.)
- Density
- 1.424 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.561(lit.)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- water: soluble (Partially miscible)(lit.)
- form
- Liquid
- Specific Gravity
- 1.424
- color
- Clear colorless to slightly yellow
- FreezingPoint
- 12.0 to 16.0 ℃
- BRN
- 1933865
- CAS DataBase Reference
- 27060-75-9(CAS DataBase Reference)
- NIST Chemistry Reference
- 2-Bromo-5-methoxytoluene(27060-75-9)
- EPA Substance Registry System
- 2-Bromo-5-methoxytoluene (27060-75-9)
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MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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2-Bromo-5-methoxytoluene Usage And Synthesis
Chemical Properties
colorless to light yellow liquid
Uses
2-bromo-5-methoxytoluene could be used to syntheis 4-bromo-3-(bromomethyl)anisole. In specifically, to a CCl4 solution (125 mL) of 2-bromo-5-methoxytoluene (0.050 mol) and NBS (0.055 mol) was added AIBN (0.001 mol), and the mixture was stirred at 80 °C for 18 h. The mixture was diluted with hexane before filtration through a Celite pad. Evaporation of the solvent and washing the residue with ethyl acetate gave 4-bromo-3-(bromomethyl)anisole.
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