2-BROMO-5-HYDROXYMETHYL-ANISOLE
- Product Name
- 2-BROMO-5-HYDROXYMETHYL-ANISOLE
- CAS No.
- 17100-64-0
- Chemical Name
- 2-BROMO-5-HYDROXYMETHYL-ANISOLE
- Synonyms
- (4-broMo-3-Methoxyphenyl)Methanol;4-Bromo-3-methoxybenzyl alcohol;2-BROMO-5-HYDROXYMETHYL-ANISOLE;Benzyl alcohol, 4-bromo-3-methoxy-;Benzenemethanol, 4-bromo-3-methoxy-
- CBNumber
- CB01519637
- Molecular Formula
- C8H9BrO2
- Formula Weight
- 217.06
- MOL File
- 17100-64-0.mol
2-BROMO-5-HYDROXYMETHYL-ANISOLE Property
- Boiling point:
- 306.8±27.0 °C(Predicted)
- Density
- 1.513±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 14.04±0.10(Predicted)
- form
- solid
- color
- Faint orange/brown
Safety
- HS Code
- 2909498090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- B711230
- Product name
- (4-Bromo-3-methoxyphenyl)methanol
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- FB142805
- Product name
- (4-Bromo-3-methoxyphenyl)methanol
- Packaging
- 250mg
- Price
- $70
- Updated
- 2021/12/16
- Product number
- FB142805
- Product name
- (4-Bromo-3-methoxyphenyl)methanol
- Packaging
- 500mg
- Price
- $125
- Updated
- 2021/12/16
- Product number
- FB142805
- Product name
- (4-Bromo-3-methoxyphenyl)methanol
- Packaging
- 1g
- Price
- $216
- Updated
- 2021/12/16
- Product number
- 2607-9-22
- Product name
- 4-Bromo-3-methoxybenzyl alcohol
- Packaging
- 1g
- Price
- $248
- Updated
- 2021/12/16
2-BROMO-5-HYDROXYMETHYL-ANISOLE Chemical Properties,Usage,Production
Synthesis
6971-51-3
17100-64-0
The general procedure for the synthesis of 2-bromo-5-hydroxymethyl anisole from m-methoxybenzyl alcohol was as follows: to a solution of 3-methoxybenzyl alcohol (20.0 g, 145 mmol) in tetrahydrofuran (THF, 400 mL) was added N-bromosuccinimide (NBS, 26 g, 146 mmol). The reaction mixture was stirred at room temperature for 8 hours. After the reaction was completed, ether (500 mL) was added to dilute and the mixture was washed with deionized water (3 x 100 mL). The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford 2-bromo-5-hydroxymethyl anisole (31.2 g, 99% yield), and the product was used directly in the next reaction without further purification.
References
[1] Patent: US9725406, 2017, B1. Location in patent: Page/Page column 7-8
[2] Tetrahedron, 2005, vol. 61, # 49, p. 11692 - 11696
[3] Patent: US2018/208604, 2018, A1. Location in patent: Paragraph 0201-0203
[4] Patent: US2010/4159, 2010, A1. Location in patent: Page/Page column 59; 64
[5] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 3, p. 1010 - 1014
2-BROMO-5-HYDROXYMETHYL-ANISOLE Preparation Products And Raw materials
Raw materials
Preparation Products
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