Basic information Safety Supplier Related

2,4-Dichloro-5-pyrimidinecarbonyl chloride

Basic information Safety Supplier Related

2,4-Dichloro-5-pyrimidinecarbonyl chloride Basic information

Product Name:
2,4-Dichloro-5-pyrimidinecarbonyl chloride
Synonyms:
  • 2,4-Dichloropyrimidine-5-carbonyl chloride
  • 2,4-Dichloro-5-pyrimidinecarbonylchloride
  • 5-(Chlorocarbonyl)-2,4-dichloropyrimidine, 5-(Chloroformyl)-2,4-dichloropyrimidine
  • 2,4-DichloropyriMidine-5-carbonyl chloride 97%
  • 5-(Chlorocarbonyl)-2,4-dichloropyrimidine
  • 2,3-Dichloro-5-pyrimidine carbonyl chloride
  • 5-(Chlorocarbonyl)-2,4-dichlo
  • 5-Pyrimidinecarbonyl chloride, 2,4-dichloro-
CAS:
2972-52-3
MF:
C5HCl3N2O
MW:
211.43
EINECS:
638-925-2
Product Categories:
  • Pyrimidine
  • Building Blocks
  • Pyrimidines
  • pharmacetical
  • Pyrimidine series
  • Heterocycle-Pyrimidine series
Mol File:
2972-52-3.mol
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2,4-Dichloro-5-pyrimidinecarbonyl chloride Chemical Properties

Boiling point:
83 °C(Press: 0.05 Torr)
Density 
1.645 g/mL at 25 °C
refractive index 
n20/D1.586
Flash point:
93℃
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
form 
liquid
pka
-5.08±0.29(Predicted)
color 
Clear, colourless
InChI
InChI=1S/C5HCl3N2O/c6-3-2(4(7)11)1-9-5(8)10-3/h1H
InChIKey
DZTIFMWYYHCREC-UHFFFAOYSA-N
SMILES
C(Cl)(C1=CN=C(Cl)N=C1Cl)=O
CAS DataBase Reference
2972-52-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
20/21/22-34
Safety Statements 
6-7/9-24/25-26-36/37/39-51
RIDADR 
3265
WGK Germany 
3
HazardClass 
IRRITANT, CORROSIVE
PackingGroup 
HS Code 
2933599590
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2,4-Dichloro-5-pyrimidinecarbonyl chloride Usage And Synthesis

Synthesis

23945-44-0

2972-52-3

The general procedure for the synthesis of 2,4-dichloro-5-pyrimidinecarbonyl chloride from uracil-5-carboxylic acid is as follows: 9.1 Preparation of 2,4-dihydroxypyrimidine-5-carbonyl chloride In a 250 mL round bottom flask, 10.0 g (64.0 mmol) of 2,4-dihydroxypyrimidine-5-carboxylic acid was dissolved in 46 mL (500.0 mmol) of phosphorus oxychloride (POCl3) under nitrogen protection. The reaction mixture was cooled to 0°C via an ice bath, followed by the batch addition of 47.7 g (230 mmol) phosphorus pentachloride (PCl5). The reaction solution was heated and stirred at reflux for 16 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in 100 mL of toluene and ground, followed by filtration. After this operation was repeated three times, the filtrate was evaporated under reduced pressure to give 13.5 g (64.0 mmol) of the yellow oily product 2,4-dichloro-5-pyrimidinecarbonyl chloride, which was used directly in the next step of the reaction. Yield = 100%.

References

[1] Patent: US2011/251194, 2011, A1. Location in patent: Page/Page column 21
[2] Patent: US2010/222319, 2010, A1. Location in patent: Page/Page column 18
[3] Patent: WO2015/21149, 2015, A1. Location in patent: Page/Page column 56; 57
[4] Journal of Medicinal Chemistry, 2015, vol. 58, # 6, p. 2746 - 2763
[5] Patent: WO2015/48662, 2015, A2. Location in patent: Page/Page column 55

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