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1-BROMO-2-NAPHTHALDEHYDE

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1-BROMO-2-NAPHTHALDEHYDE Basic information

Product Name:
1-BROMO-2-NAPHTHALDEHYDE
Synonyms:
  • 1-bromo-2-naphthaldehyde crystalline
  • 1-BROMO-2-NAPHTHALDEHYDE
  • 1-BROMONAPHTHALENE-2-CARBALDEHYDE
  • 1-BROMO-2-NAPHTHALDEHYDE 96+%
  • 1-Bromo-2-naphthalenecarbaldehyde
  • 1-Bromo-2-naphthalenecarboxaldehyde
  • 1-broMo-2-phthaldehyde
  • 1-Bromo-2-naphthaldehyde >=96.0% (HPLC)
CAS:
3378-82-3
MF:
C11H7BrO
MW:
235.08
EINECS:
222-180-1
Product Categories:
  • oled
Mol File:
3378-82-3.mol
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1-BROMO-2-NAPHTHALDEHYDE Chemical Properties

Melting point:
118°C
Boiling point:
347℃
Density 
1.552
Flash point:
120℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
crystals
Appearance
Off-white to yellow Solid
BRN 
2613639
InChI
InChI=1S/C11H7BrO/c12-11-9(7-13)6-5-8-3-1-2-4-10(8)11/h1-7H
InChIKey
CYGUXEZVBLMVRV-UHFFFAOYSA-N
SMILES
C1(Br)=C2C(C=CC=C2)=CC=C1C=O
CAS DataBase Reference
3378-82-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29130000

MSDS

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1-BROMO-2-NAPHTHALDEHYDE Usage And Synthesis

Chemical Properties

Light yellow solid

Uses

1-Bromo-2-naphthaldehyde is used as a reagent in the synthesis of Hoveyda-Grubbs type metathesis catalysts which are used in cross olefin metathesis. 1-Bromo-2-naphthaldehyde is also used in the preparation of novel (-)-cercosporamide derivatives as potent selective PPARγ modulators.

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 4617, 1981 DOI: 10.1021/jo00335a076

Synthesis

37763-43-2

3378-82-3

General procedure for the synthesis of 1-bromo-2-naphthalene formaldehyde from 1-bromo-2-(bromomethyl)naphthalene: In a 2L reactor, 4-methylmorpholine N-oxide (61.4 g, 524 mmol), molecular sieves (200 g) and acetonitrile (1.2 L) were added and stirred for 30 min at 0 °C under nitrogen protection. Subsequently, 1-bromo-2-(bromomethyl)naphthalene (78 g, 262 mmol) was added and stirring was continued for 6 hours at room temperature. After completion of the reaction, the reaction mixture was filtered and the filtrate was washed with dichloromethane. The filtrate was concentrated and purified by column chromatography to afford 1-bromo-2-naphthaldehyde (45 g) in 73% yield.

References

[1] European Journal of Organic Chemistry, 2012, # 31, p. 6155 - 6164,10
[2] European Journal of Organic Chemistry, 2012, # 31, p. 6155 - 6164
[3] Tetrahedron Letters, 1994, vol. 35, # 48, p. 8985 - 8988
[4] Patent: US2018/72753, 2018, A1. Location in patent: Paragraph 0163-0164
[5] Journal of the Chemical Society, Perkin Transactions 1, 2000, # 9, p. 1363 - 1378

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