2-Chloropyrimidine

2-Chloropyrimidine
  • CAS No.:1722-12-9
Other grades of this product :
2-Chloropyrimidine Chemical Properties
Melting point 63-66 °C (lit.)
Boiling point 75-76 °C/10 mmHg (lit.)
density 1.2710 (rough estimate)
refractive index 1.5320 (estimate)
Fp 98 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Methanol, Water
pka-1.46±0.13(Predicted)
form Crystals or Crystalline Powder
color Yellow to pale orange
Water Solubility Slightly soluble in water. 33.3 mg soluble in 1 mL of alcohol.
Sensitive Moisture Sensitive
BRN 107171
InChIKeyUNCQVRBWJWWJBF-UHFFFAOYSA-N
CAS DataBase Reference1722-12-9(CAS DataBase Reference)
NIST Chemistry ReferencePyrimidine, 2-chloro-(1722-12-9)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36-36/38-36/37/38
Safety Statements 26-37/39-36
RIDADR 2811
WGK Germany 3
10-23
Hazard Note Irritant
HazardClass 6.1(b)
PackingGroup III
HS Code 29339900
MSDS Information
ProviderLanguage
2-Chloropyrimidine English
SigmaAldrich English
ACROS English
ALFA English
2-Chloropyrimidine Usage And Synthesis
Chemical Propertiesyellowish to pale orange crystals or cryst. powder
Uses2-Chloropyrimidine is a monochlorinated pyrimidine with plant growth regulating activity. Chloropyrimidine is a useful reagent in the preparation of antivirals and other biologically active compounds.
Uses2-Chloropyrimidine is a useful reagent in the preparation of antivirals and other biologically active compounds. It was used in the synthesis of 4?-(1,1?-(5-(2-methoxyphenoxy)-[2,2?-bipyrimidine]-4,6-diyl)bis(1H-pyrazol-3,1-diyl)) dianiline fluorescent dye, biosensor for protein assay, 2-amino-4-heteroarylpyrimidines, cis- and trans-octahydropyrrolo[2,3]pyridine derivatives.
General Description2-Chloropyrimidine undergoes cobalt-catalyzed cross-coupling reaction with aryl halides.
Purification MethodsIt has been recrystallised from *C6H6, pet ether or a mixture of both. It sublimes at 50o/18mm and can be distilled in a vacuum. [IR: Short & Thompson J Chem Soc 168 1952, Boarland & McOmie J Chem Soc 1218 1951, Beilstein 23/5 V 343.]

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