3-BroMo-4-fluorobenzyl alcohol

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3-BroMo-4-fluorobenzyl alcohol Basic information
Uses
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-fluorobenzenemethanol;3-Bromo-4-fluorobenzyl Alcohol >;Benzenemethanol, 3-bromo-4-fluoro-;Enzalutamide Impurity 37;(3-BROMO-4-FLUORO-PHENYL)-METHANOL
CAS:77771-03-0
MF:C7H6BrFO
MW:205.02
EINECS:
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
3-BroMo-4-fluorobenzyl alcohol Structure
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
pka13.83±0.10(Predicted)
form Powder
color Yellow
Water Solubility soluble
CAS DataBase Reference77771-03-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39-24/25
Hazard Note Irritant
HS Code 29214900
MSDS Information
3-BroMo-4-fluorobenzyl alcohol Usage And Synthesis
Uses3-Bromo-4-fluorobenzylamine hydrochloride is a pharmaceutical intermediate and an important intermediate for the synthesis of alkylbenzylamine derivatives.
Chemical PropertiesYELLOW POWDER
SynthesisThe 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 32C, 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 alcohol Preparation Products And Raw materials
Preparation ProductsBenzonitrile, 2-fluoro-5-(hydroxymethyl)- (9CI)-->3-Bromo-4-fluorobenzaldehyde
Tag:3-BroMo-4-fluorobenzyl alcohol(77771-03-0) Related Product Information
Ethyl bromodifluoroacetate Trimethoprim Phenoxybenzamine hydrochloride 4-Fluorobenzylamine 3-Bromoanisole Topotecan hydrochloride Benzylamine hydrochloride DL-alpha-Methylbenzylamine 4-Bromophenylhydrazine hydrochloride 3-Bromo-4-fluorobenzoic acid 3-Bromo-2,4,5-trifluorobenzoic acid 3-BROMO-5-FLUOROBENZYLAMINE HYDROCHLORIDE,4-BROMO-2-FLUOROBENZYLAMINE HYDROCHLORIDE,4-Bromo-2-fluorobenzylamine hydrochloride 98% 4-Fluorobenzyl alcohol Bromine 5-Bromo-2-fluorobenzyl alcohol cis-Ferulicacid 3-Bromo-4-fluoro-benzoic acid methyl ester Bromotrifluoromethane