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PYRIMIDINE-4-CARBOXALDEHYDE

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CAS:2435-50-9
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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CAS:2435-50-9
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CAS:2435-50-9
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CAS:2435-50-9
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-01243
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Products Intro: Product Name:pyrimidine-4-carboxaldehyde
CAS:2435-50-9
Purity:0.99 Package:1kg

PYRIMIDINE-4-CARBOXALDEHYDE manufacturers

  • pyriMidine-4-carboxaldehyde
  • pyriMidine-4-carboxaldehyde pictures
  • $15.00 / 1KG
  • 2021-07-02
  • CAS:2435-50-9
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
PYRIMIDINE-4-CARBOXALDEHYDE Basic information
Uses
Product Name:PYRIMIDINE-4-CARBOXALDEHYDE
Synonyms:4-PYRIMIDINE CARBALDEHYDE;RARECHEM AK ML 0567;PYRIMIDINE-4-CARBOXALDEHYDE;4-Pyrimidinecarboxaldehyde;4-Pyrimidinecarboxaldehyde (7CI,8CI,9CI);4-Formylpyrimidine, 4-Formyl-1,3-diazine;PYRIMIDINE-4-CARBOXALDEHYDE ISO 9001:2015 REACH
CAS:2435-50-9
MF:C5H4N2O
MW:108.1
EINECS:
Product Categories:Heterocycle-Pyrimidine series;pharmacetical;PYRIMIDINE;Pyrimidine series
Mol File:2435-50-9.mol
PYRIMIDINE-4-CARBOXALDEHYDE Structure
PYRIMIDINE-4-CARBOXALDEHYDE Chemical Properties
Boiling point 225.3±13.0 °C(Predicted)
density 1.234±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
form liquid
pka-0.14±0.10(Predicted)
color Clear, faint yellow
InChIInChI=1S/C5H4N2O/c8-3-5-1-2-6-4-7-5/h1-4H
InChIKeyOKULHRWWYCFJAB-UHFFFAOYSA-N
SMILESC1=NC=CC(C=O)=N1
Safety Information
RIDADR 1993
HazardClass 3
PackingGroup 
HS Code 2933599590
MSDS Information
PYRIMIDINE-4-CARBOXALDEHYDE Usage And Synthesis
UsesPyrimidine-4-carboxaldehyde is an aldehyde derivative that can be used as a pharmaceutical intermediate.
Synthesis
4-Methylpyrimidine

3438-46-8

PYRIMIDINE-4-CARBOXALDEHYDE

2435-50-9

Method G: Synthesis of the intermediate 7(1-7) - pyrimidine-4-carbaldehyde. To a 10 mL solution of dioxane containing 1.0 g (10 mmol, 1.0 eq.) of 4-methylpyrimidine was added 1.2 g (10 mmol, 1.0 eq.) of selenium dioxide. The reaction mixture was heated at 100 °C for 5 hours and subsequently cooled to room temperature. After the addition of 0.25 g (2.3 mmol, 0.23 eq.) of selenium dioxide was made up, the heating was continued at 100 °C for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and filtered through Celite. The filter cake was washed with 200 mL of ethyl acetate, and the filtrates were combined and concentrated under vacuum. The resulting dark brown oil was suspended with 200 mL of dichloromethane and filtered. Finally, the solvent was removed by vacuum to give 0.3 g (2.8 mmol, 28% yield) of pyrimidine-4-carbaldehyde (1-7) as a dark brown oily product.

References[1] Heterocycles, 2003, vol. 60, # 4, p. 953 - 957
[2] Patent: WO2007/104053, 2007, A2. Location in patent: Page/Page column 36
[3] Patent: US2003/125339, 2003, A1
[4] Patent: EP150984, 1991, B1
[5] Patent: US4826833, 1989, A
PYRIMIDINE-4-CARBOXALDEHYDE Preparation Products And Raw materials
Raw materials4-(DIMETHOXYMETHYL)PYRIMIDINE-->4-Methylpyrimidine-->Selenium dioxide-->1,4-Dioxane
Preparation ProductsPyrimidine, 4-methyl-, 1-oxide (6CI,7CI,8CI,9CI)-->4-Pyrimidinecarboxylic acid
Tag:PYRIMIDINE-4-CARBOXALDEHYDE(2435-50-9) Related Product Information
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