Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Ketones >  3,5-Dibromoacetophenone

3,5-Dibromoacetophenone

Basic information Uses Safety Supplier Related

3,5-Dibromoacetophenone Basic information

Product Name:
3,5-Dibromoacetophenone
Synonyms:
  • 1-(3,5-dibromophenyl)ethan-1-one
  • 3,5-DIBROMOACETOPHENONE
  • 3,5-DIBROMOACETOPHENONE 99%MIN
  • Ethanone, 1-(3,5-dibromophenyl)-
  • Acetophenone, 3',5'-dibromo-
  • 3',5'-Dibromoacetophenone
  • 3,5-Dibromophenacylchloride
CAS:
14401-73-1
MF:
C8H6Br2O
MW:
277.94
Product Categories:
  • Aromatic Acetophenones & Derivatives (substituted)
  • Adehydes, Acetals & Ketones
  • Bromine Compounds
  • organic chemicals and derivatives/others
  • OLED
Mol File:
14401-73-1.mol
More
Less

3,5-Dibromoacetophenone Chemical Properties

Melting point:
68°C
Boiling point:
160-164 °C(Press: 1-2 Torr)
Density 
1.7855 (rough estimate)
refractive index 
1.5560 (estimate)
storage temp. 
Sealed in dry,Room Temperature
Appearance
Off-white to yellow Solid
InChI
InChI=1S/C8H6Br2O/c1-5(11)6-2-7(9)4-8(10)3-6/h2-4H,1H3
InChIKey
NHFJDRRYVMJBRJ-UHFFFAOYSA-N
SMILES
C(=O)(C1=CC(Br)=CC(Br)=C1)C
More
Less

Safety Information

HS Code 
2914500090
More
Less

3,5-Dibromoacetophenone Usage And Synthesis

Uses

3',5'-Dibromoacetophenone is a useful research chemical.

Description

3,5-Dibromoacetophenone is a halogenated acetophenone compound containing bromine functional groups at positions 3 and 5. It can be used with halogenated metal salts as raw materials to prepare a polyhalogenated thiazolinone compound.

Synthesis

127-19-5

14401-73-1

General procedure for the synthesis of 3,5-dibromoacetophenone: To a round-bottomed flask containing 1,3,5-tribromobenzene (6.3 g, 20 mmol) and anhydrous ethyl ether (150 mL) under nitrogen protection, a n-butyllithium solution (12.5 mL, 20 mmol) was slowly added at -78 °C and stirred for 2 h at this temperature. Subsequently, a solution of N,N-dimethylacetamide (1.92 g, 22 mmol) in anhydrous ether (15 mL) was added dropwise. The reaction mixture was slowly warmed from -78°C to room temperature and stirring was continued for 20 hours. Upon completion of the reaction, extraction was carried out with ether and the solvent was removed by distillation after combining the organic phases. The product was purified by column chromatography and recrystallization to give 3,5-dibromoacetophenone in 41% yield.

References

[1] Patent: US2007/138945, 2007, A1. Location in patent: Page/Page column 11

3,5-DibromoacetophenoneSupplier

Hubei Deli Pharmaceutical Technology Co., Ltd Gold
Tel
13372285931
Email
52519240@qq.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Email
sales@accelachem.com
Shanghai Harvest Chemical Industrial Co., Ltd.
Tel
021-31038972,31038973 17321035817
Email
sales@harvest-chem.com