Basic information Safety Supplier Related

7-Bromo-1-tetralone

Basic information Safety Supplier Related

7-Bromo-1-tetralone Basic information

Product Name:
7-Bromo-1-tetralone
Synonyms:
  • NSC 74917
  • 7-BROMO-3,4-DIHYDRO-1(2H)-NAPHTHALENONE
  • 7-BROMO-3,4-DIHYDRO-2H-NAPHTHALEN-1-ONE
  • 7-BROMO-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE
  • 7-BROMO-1-TETRALONE
  • 7-Bromo-3,4-dihydro-2H-phthalen-1-one
  • 7-bromo-1-tetralin-one
  • 7-BROMOTETRALONE
CAS:
32281-97-3
MF:
C10H9BrO
MW:
225.08
Product Categories:
  • Building Blocks
  • C10
  • Carbonyl Compounds
  • Chemical Synthesis
  • Ketones
  • Organic Building Blocks
  • Benzocycles
Mol File:
32281-97-3.mol
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7-Bromo-1-tetralone Chemical Properties

Melting point:
78 °C
Boiling point:
157°C/8mmHg(lit.)
Density 
1.511±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Light yellow to Dark green
λmax
305nm(EtOH)(lit.)
InChI
InChI=1S/C10H9BrO/c11-8-5-4-7-2-1-3-10(12)9(7)6-8/h4-6H,1-3H2
InChIKey
YGVDCGFUUUJCDF-UHFFFAOYSA-N
SMILES
C1(=O)C2=C(C=CC(Br)=C2)CCC1
CAS DataBase Reference
32281-97-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39-24/25
WGK Germany 
2
HazardClass 
IRRITANT
HS Code 
29147000
Storage Class
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Oral
Aquatic Chronic 3

MSDS

  • Language:English Provider:ALFA
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7-Bromo-1-tetralone Usage And Synthesis

Chemical Properties

White to yellow to tan powder or crystal

Uses

7-Bromo-1-tetralone is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Synthesis

A mixture of 4-(8-methoxynaphthalen-2-yl)-2-methyl-1,2,3,4-tetrahydroisoquinoline maleate (57 g, 223 mmol), potassium hydroxide (43 g, 760 mmol), and hydrazine hydrate (26 m1, 830 mmol) in diethylene glycol (2,865 ml) was stirred for 3 hr at 195 ??C. After cooling to below 40??C, the mixture was diluted with water (300 ml), poured into 3 M NaOH and washed three times with dichloromethane. Brine was added to break up the emulsion. The aqueous layer was acidified to pH 1 with 6M HCl and extracted three times with methyl tert-butyl ether. The combined organic extracts were dried with magnesium sulfate to give 4-(4-bromophenyl)butyric acid (41 g, 75%). The product of the previous step (97 g, 397 mmol) was added to polyphosphoric acid (580 g) and the resulting mixture was stirred at 90??C for 10 min. After cooling to 0??C, 6 M NaOH was added and the mixture was extracted with methyl tert-butyl ether. The organic extract was dried with magnesium sulfate to give 7-bromo-3,4-dihydronaphthalen-1-one (49 g, 55%), chromatographed (6:1 to 4:1 heptane/ethyl acetate) and recrystallized from cyclohexane to give the product 7-bromo-3,4-dihydro-2H-1-naphthalenone.

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