5-BROMO-2-METHOXYBENZYL ALCOHOL
5-BROMO-2-METHOXYBENZYL ALCOHOL Basic information
- Product Name:
- 5-BROMO-2-METHOXYBENZYL ALCOHOL
- Synonyms:
-
- RARECHEM AL BD 0053
- BenzeneMethanol, 5-broMo-2-Methoxy-
- 5-BroMo-2-Methoxybenzyl alcohol, 97% 5GR
- 5-Brom-2-methoxybenzyl alcohol
- 5-Bromo-2-methoxybenzyl alcohol 98%
- 5-BROMO-O-ANISYL ALCOHOL
- 5-BROMO-2-METHOXYBENZYL ALCOHOL
- (5-BROMO-2-METHOXY-PHENYL)-METHANOL
- CAS:
- 80866-82-6
- MF:
- C8H9BrO2
- MW:
- 217.06
- EINECS:
- 279-586-7
- Product Categories:
-
- Benzhydrols, Benzyl & Special Alcohols
- Alcohol
- Alcohols
- Anisoles, Alkyloxy Compounds & Phenylacetates
- Bromine Compounds
- C7 to C8
- Oxygen Compounds
- Mol File:
- 80866-82-6.mol
5-BROMO-2-METHOXYBENZYL ALCOHOL Chemical Properties
- Melting point:
- 68-71 °C (lit.)
- Boiling point:
- 192.5°C (rough estimate)
- Density
- 1.4816 (rough estimate)
- refractive index
- 1.4930 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- color
- White to Light yellow
- CAS DataBase Reference
- 80866-82-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xn,Xi
- Risk Statements
- 36/37/38-22
- Safety Statements
- 37/39-26-24/25
- WGK Germany
- 3
- Hazard Note
- Irritant
- HS Code
- 29094990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
5-BROMO-2-METHOXYBENZYL ALCOHOL Usage And Synthesis
Chemical Properties
white to light yellow crystal powder
Uses
5-Bromo-2-methoxybenzyl alcohol has been used in the synthesis of 5-bromo-2-methoxyphenylacetic acid.
Synthesis
612-16-8
80866-82-6
GENERAL METHODS: Lithium bromide monohydrate (0.2 mmol) and iodobenzene diacetate (0.2 mmol) were added to a solution of 2-methoxybenzenemethanol (0.2 mmol) in trifluoroethanol (1 mL) and the reaction was carried out at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous sodium sulfite solution. The mixture was extracted with dichloromethane and the combined organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure and the residue was purified by silica gel column chromatography to afford the target product 5-bromo-2-methoxybenzyl alcohol.
References
[1] Synlett, 2018, vol. 29, # 17, p. 2275 - 2278
[2] Tetrahedron Letters, 2000, vol. 41, # 46, p. 8881 - 8885
[3] Synthetic Communications, 2007, vol. 37, # 9, p. 1571 - 1577
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5-BROMO-2-METHOXYBENZYL ALCOHOL(80866-82-6)Related Product Information
- 5-BROMO-2-METHOXYPHENYLACETIC ACID
- 5-BROMO-2-METHOXY-NICOTINIC ACID
- 5-Bromo-2-methoxybenzoic acid
- 3-BROMO-5-CHLORO-2,6-DIMETHOXYBENZOIC ACID
- Acid Red 92
- METHYL 3,5-DIBROMO-2,4-DIMETHOXY-6-METHYLBENZOATE
- 3-BROMO-2,6-DIMETHOXYBENZOIC ACID
- Bromopyrogallol Red
- 5-BROMO-2-METHOXYBENZYL ALCOHOL
- 2',4',5',7'-TETRABROMO-3,4,5,6-TETRACHLOROFLUORESCEIN
- Acid Red 87
- 4-BROMO-2-METHOXYBENZYL ALCOHOL 97
- 2-Methoxybenzyl alcohol
- EOSIN
- EOSIN 5-ISOTHIOCYANATE
- TETRACHROME STAIN
- 3,5-DIBROMO-2-METHOXYBENZOIC ACID
- AZUR C EOSINATE