2-BROMO-1-PHENYL-PENTAN-1-ONE

Superiority:

Chinese name 2-bromo-1-phenyl-1-pentanone Chinese synonym 2-bromo-1-phenyl-1-pentanone; Α-BROMOVALEROPHENONE; 2-bromo-1-phenyl-1-pentanone raw material; 49851312TELEGRAMJESSIEAOKSBIO; Pseudo ROMOVALEROPHENONE; Α-BROMOVALEROPHENONEWICKRJANE8886; 2-bromo-1-phenylpentan-1-one; 2-bromo-1-phenyl-1-pentanone Grade 8 English name 2-Bromo-1-phenyl-pentan-1-one English synonym alpha-bromovaliropheone; 2-Bromo-1-phenyl-1-pentanone,2-Bromovalerophenone; 2-BROMO-1-PHENYL-PENTAN-1-ONE; 2-BroMovalerophenone; China2-bromo-1-phenylpentan-1-one; 2-Bromo-1-Phenyl-1-PentanoneCAS49851-31-2kf-wang(at)kf-chem.com; 2-BROMO-1-PHENYL-1-PENTANONE; 2-Bromovalerophenone alpha Bromovalerophenone CAS number 49851-31-2 Molecular formula C11H13BrO Molecular weight 241.12 EINECS number 100-201-4 Related category organic intermediate; Chemical raw materials; Intermediate of synthetic materials; Chemical intermediates; Pharmaceutical raw materials; Already esterified; Aromatics; InhibitorsChemicalbook; Intermediates&FineChemicals; Pharmaceuticals; Chemical; 49851-31-2; PharmMol file 49851-31-2.mol structural formula 2-bromo-1-phenyl-1-pentanone properties boiling point 94-96 ° C (Press: 0.25Torr) density 1.310 ± 0.06g/cm3 (Predicted) storage conditions -20 ° C Freezer solubility soluble in chloroform (a little), methanol (a little) form oily color transparent colorless InChIInChI=1S/C11H13BrO/c1-2-6-10(12)11(13)9-7-4-3-5-8-9/h3-5,7-8,10H,2,6H2,1H3InChIKeyXOQFMNXQYSTQPE-UHFFFAOYSA-NSMILESC(C1=CC=CC=C1)(=O)C(Br)CCC2- Application and synthesis method of bromo-1-phenyl-1-pentanone: 2-bromo-1-phenyl-1-pentanone is a white crystalline powder and a derivative of valerone. Can be used as a pharmaceutical intermediate. At room temperature, 16.2g (0.1mol) of benzophenone and 30.9g (0.3mol) of sodium bromide were added to a 500mL round bottom flask, respectively. After stirring evenly, 24g (0.2mol) of 30% hydrochloric acid was added, and 19g (0.15mol) of 30% hydrogen peroxide was slowly added dropwise. After the dropwise addition was completed, the reaction was continued for 1-2 hours. After TLC monitoring of the reaction was completed, stirring was stopped, and the layers were allowed to stand. The organic phases were washed separately with saturated sodium carbonate and saturated saline solution, combined, concentrated, and dried over anhydrous magnesium sulfate to obtain 2-bromo-1-phenyl-1-pentanone, a bright yellow oily liquid with a yield of 95% and a purity of 98% (HPLC method).

We can provide free samples to your company, 500ml samples, please add my contact information