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4-Bromo-3-fluorobenzaldehyde

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4-Bromo-3-fluorobenzaldehyde Basic information

Product Name:
4-Bromo-3-fluorobenzaldehyde
Synonyms:
  • 4-BROMO-3-FLUOROBENZALDEHYDE
  • 4-Bromo-3-fluorobenzaldehyde 98%
  • 4-Bromo-3-fluorobenzaldehyde98%
  • 3-Fluoro-4-bromobenzaldehyde
  • Benzaldehyde, 4-broMo-3-fluoro-
  • 4-BroMo-3-fluorobenzaldehyde, 95+%
  • 4 - broMine - 3 - fluoro benzaldehyde
  • 4-Bromo-3-fluorobenzaldehyde >
CAS:
133059-43-5
MF:
C7H4BrFO
MW:
203.01
Product Categories:
  • Aldehydes
  • Aryl Fluorinated Building Blocks
  • Building Blocks
  • C7
  • Carbonyl Compounds
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • Benzaldehyde
  • Miscellaneous
  • Aromatic Aldehydes & Derivatives (substituted)
Mol File:
133059-43-5.mol
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4-Bromo-3-fluorobenzaldehyde Chemical Properties

Melting point:
55-59 °C
Boiling point:
240.2±25.0 °C(Predicted)
Density 
1.670±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Light yellow
InChI
InChI=1S/C7H4BrFO/c8-6-2-1-5(4-10)3-7(6)9/h1-4H
InChIKey
SWHUROFMIMHWKS-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=C(Br)C(F)=C1
CAS DataBase Reference
133059-43-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-36-22
Safety Statements 
26-36/37/39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29130000
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4-Bromo-3-fluorobenzaldehyde Usage And Synthesis

Chemical Properties

White powder

Uses

4-Bromo-3-fluorobenzaldehyde is used in preparation of the Deuterated Dihydropyrimidine compound and their application as anti-HBV agent.

Synthesis

222978-01-0

133059-43-5

General procedure for the synthesis of 3-fluoro-4-bromobenzaldehyde from 4-bromo-3-fluorobenzyl alcohol: Manganese dioxide (18.7 g, 210 mmol) was added to a solution of 4-bromo-3-fluorobenzyl alcohol (4.3 g, 21 mmol) in chloroform (50 mL), and the reaction mixture was stirred at 37 °C overnight. The progress of the reaction was monitored by thin layer chromatography (TLC) until the raw material was completely consumed. Upon completion of the reaction, the mixture was filtered and the filtrate was concentrated under reduced pressure to afford the target product 3-fluoro-4-bromobenzaldehyde (2.3 g, 55% yield).

References

[1] Patent: US2010/216806, 2010, A1. Location in patent: Page/Page column 103
[2] Patent: US6297239, 2001, B1

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