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5-fluoropyriMidine-2-carbaldehyde

Product Name
5-fluoropyriMidine-2-carbaldehyde
CAS No.
935667-50-8
Chemical Name
5-fluoropyriMidine-2-carbaldehyde
Synonyms
5-fluoropyriMidine-2-carbaldehyde;5-FluoropyriMidine-2-carboxaldehyde;5-Fluoro-2-pyrimidinecarboxaldehyde;2-Pyrimidinecarboxaldehyde, 5-fluoro-
CBNumber
CB52616534
Molecular Formula
C5H3FN2O
Formula Weight
126.09
MOL File
935667-50-8.mol
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5-fluoropyriMidine-2-carbaldehyde Property

Boiling point:
272.3±32.0 °C(Predicted)
Density 
1.374±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-2.22±0.22(Predicted)
Appearance
Orange to red Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
F600100
Product name
5-Fluoropyrimidine-2-carbaldehyde
Packaging
50mg
Price
$310
Updated
2021/12/16
AK Scientific
Product number
3220AJ
Product name
5-Fluoropyrimidine-2-carbaldehyde
Packaging
1g
Price
$1268
Updated
2021/12/16
Matrix Scientific
Product number
122461
Product name
5-Fluoropyrimidine-2-carboxaldehyde
Purity
97.0%
Packaging
1g
Price
$1980
Updated
2021/12/16
SynQuest Laboratories
Product number
4H15-3-37
Product name
5-Fluoropyrimidine-2-carbaldehyde
Purity
97%
Packaging
1g
Price
$2267
Updated
2021/12/16
SynQuest Laboratories
Product number
4H15-3-37
Product name
5-Fluoropyrimidine-2-carbaldehyde
Purity
97%
Packaging
250mg
Price
$843
Updated
2021/12/16
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5-fluoropyriMidine-2-carbaldehyde Chemical Properties,Usage,Production

Synthesis

38275-55-7

935667-50-8

General procedure for the synthesis of 5-fluoropyrimidine-2-carbaldehyde from 2-cyano-5-fluoropyrimidine: To an anhydrous THF solution of 5-fluoropyrimidine-2-carbonitrile (1.0 g, 8.1 mmol) was slowly added a solution of DIBAL-H (8.1 mL) over a period of 20 min at -78 °C. The reaction mixture was continued to be stirred at this temperature for 2 h. The reaction was subsequently quenched by the addition of MeOH. The reaction system was slowly warmed to room temperature and then concentrated HCl solution was added. The resulting mixture was stirred at room temperature for 2 h before being extracted with an aqueous layer and EtOAc (3 times). The combined organic phases were washed with brine and dried over MgSO4. The solvent was removed by concentration under reduced pressure to give 5-fluoropyrimidine-2-carbaldehyde (780 mg, 76% yield). Mass spectrometry result: [M+H]+ 127.

References

[1] Patent: WO2007/49041, 2007, A1. Location in patent: Page/Page column 71
[2] Patent: WO2008/117050, 2008, A1. Location in patent: Page/Page column 64
[3] Patent: WO2008/135786, 2008, A1. Location in patent: Page/Page column 53
[4] Patent: WO2013/142269, 2013, A1. Location in patent: Paragraph 0645; 0646; 0647

5-fluoropyriMidine-2-carbaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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935667-50-8, 5-fluoropyriMidine-2-carbaldehydeRelated Search:


  • 5-fluoropyriMidine-2-carbaldehyde
  • 5-FluoropyriMidine-2-carboxaldehyde
  • 2-Pyrimidinecarboxaldehyde, 5-fluoro-
  • 5-Fluoro-2-pyrimidinecarboxaldehyde
  • 935667-50-8
  • C5H3FN2O