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4-Acetyl-4'-bromobiphenyl

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4-Acetyl-4'-bromobiphenyl Basic information

Product Name:
4-Acetyl-4'-bromobiphenyl
Synonyms:
  • AKOS BAR-2458
  • 4-ACETYL-4'-BROMOBIPHENYL
  • 4-ACETYL-4'-BROMODIPHENYL
  • 4'-(P-BROMOPHENYL)ACETOPHENONE
  • 4'-(4-BROMOPHENYL)ACETOPHENONE
  • 4'-(4-Bromophenyl)acetophenone Synonyms 4-Acetyl-4'-bromobiphenyl
  • TIMTEC-BB SBB005889
  • 4-(4-BROMOPHENYL)ACETOPHENONE
CAS:
5731-01-1
MF:
C14H11BrO
MW:
275.14
EINECS:
227-236-9
Product Categories:
  • Building Blocks
  • C13 to C14
  • Aromatic Halides (substituted)
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Biphenyl & Diphenyl ether
  • Electronic Chemicals
  • Bromine Compounds
  • Biphenyls (Building Blocks for Liquid Crystals)
  • Building Blocks for Liquid Crystals
  • C13 to C14
  • Carbonyl Compounds
  • Ketones
  • Functional Materials
  • 1
Mol File:
5731-01-1.mol
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4-Acetyl-4'-bromobiphenyl Chemical Properties

Melting point:
129-133 °C(lit.)
Boiling point:
372.1±17.0 °C(Predicted)
Density 
1.359±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Toluene
form 
powder to crystal
color 
White to Orange to Green
BRN 
2048590
InChI
InChI=1S/C14H11BrO/c1-10(16)11-2-4-12(5-3-11)13-6-8-14(15)9-7-13/h2-9H,1H3
InChIKey
UUVKNCRMWPNBNM-UHFFFAOYSA-N
SMILES
C(=O)(C1=CC=C(C2=CC=C(Br)C=C2)C=C1)C
CAS DataBase Reference
5731-01-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,N
Risk Statements 
36-51/53
Safety Statements 
26-36-61-24/25-22
RIDADR 
UN 3077 9/PG 3
WGK Germany 
3
HS Code 
2914790090

MSDS

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4-Acetyl-4'-bromobiphenyl Usage And Synthesis

Chemical Properties

White or pale brown solid

Uses

4-Acetyl-4'-bromobiphenyl is mainly used as a reagent for experimental organic synthesis or reactions, including substitution reactions or the synthesis and polymerisation of biphenyl derivatives.

Synthesis

Dichloromethane was added to Aluminium chloride. The mixture was stirred and cooled to 5 °C in a salt/ice bath. Acetyl chloride was quickly added through a dropping funnel and cooled to ? 3 °C to give a transparent yellow solution. Solid 4-bromobiphenyl was added in small amounts and stirred; wait for ? an hour, then add more. The mixture was stirred for ten hours, rising to 15 °C. The mixture was poured into a bucket of ice /37 percent HCl to destroy the aluminum chloride, then transferred to a separatory funnel and extracted into DCM. Then, the mixture was washed twice with water to destroy HCl. Again, it was washed with 10 percent NaOH and water. The collected DCM layer was dried over magnesium sulfate, mostly filtered by gravity. The solvent was removed in vacuo, and the residue was re-crystallized through ethanol to yield 4-Acetyl-4'-bromobiphen

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