Basic information Uses Safety Supplier Related

3-BroMo-4-fluorobenzyl alcohol

Basic information Uses Safety Supplier Related

3-BroMo-4-fluorobenzyl alcohol Basic information

Product Name:
3-BroMo-4-fluorobenzyl alcohol
Synonyms:
  • 3-Bromo-4-fluorobenzyl alcohol 99%
  • RARECHEM AL BD 0277
  • 3-BROMO-4-FLUOROBENZYL ALCOHOL
  • (3-BROMO-4-FLUORO-PHENYL)-METHANOL
  • 3-Bromo-4-fluorobenzenemethanol
  • 3-Bromo-4-fluorobenzyl Alcohol >
  • Benzenemethanol, 3-bromo-4-fluoro-
  • Enzalutamide Impurity 37
CAS:
77771-03-0
MF:
C7H6BrFO
MW:
205.02
Product Categories:
  • Alcohols
  • Bromine Compounds
  • Benzhydrols, Benzyl & Special Alcohols
  • Anilines, Aromatic Amines and Nitro Compounds
  • Fluorine series
  • Fluorine Compounds
  • Anilines, Amides & Amines
Mol File:
77771-03-0.mol
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3-BroMo-4-fluorobenzyl alcohol Chemical Properties

Melting point:
214 °C
Boiling point:
80°C/0.5mm
Density 
1.658±0.06 g/cm3(Predicted)
refractive index 
1.5590 to 1.5630
storage temp. 
Sealed in dry,Room Temperature
pka
13.83±0.10(Predicted)
form 
Powder
color 
Yellow
Water Solubility 
soluble
CAS DataBase Reference
77771-03-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-24/25
Hazard Note 
Irritant
HS Code 
29214900
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3-BroMo-4-fluorobenzyl alcohol Usage And Synthesis

Uses

3-Bromo-4-fluorobenzylamine hydrochloride is a pharmaceutical intermediate and an important intermediate for the synthesis of alkylbenzylamine derivatives.

Chemical Properties

YELLOW POWDER

Synthesis

The resulting oxime was added to a 100 mL three-necked flask with 66 mL of 15% NaOH solution, and 6.50 g of Raney nickel was added slowly in batches at a controlled temperature of 32??C, and the reaction was heated to reflux at 100 DD for 15 h. After the reaction was complete, the reaction was cooled to room temperature, and the filtration was carried out under vacuum. A small amount of water (about 5mL) was measured to wash the filtrate and the filtrate was retained. Then the filtrate was extracted with 165mL of ethyl acetate in three portions, retaining the organic oil phase layer, hydrochloric acid adjusted the pH to 1-2, and anhydrous sodium sulfate was added to it, and it was left to dry for 2 h. Vacuum filtration was carried out to obtain 3-bromo-4-fluorobenzylamine hydrochloride.

3-BroMo-4-fluorobenzyl alcoholSupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
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