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2,4,6-Trichloropyrimidine, 98%
2,4,6-Trichloropyrimidine, 98%
2,4,6-Trichloropyrimidine, 98%
Thermo Scientific Chemicals

2,4,6-Trichloropyrimidine, 98%

CAS: 3764-01-0 | C4HCl3N2 | 183.416 g/mol
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Catalog number A12842.22
also known as A12842-22
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Quantity:
100 g
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Price (USD)
206.65
Online Exclusive
229.00
Save 22.35 (10%)
Each
Chemical Identifiers
CAS3764-01-0
IUPAC Name2,4,6-trichloropyrimidine
Molecular FormulaC4HCl3N2
InChI KeyDPVIABCMTHHTGB-UHFFFAOYSA-N
SMILESClC1=CC(Cl)=NC(Cl)=N1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.5675-1.5715 @ 20?C
FormLiquid
Assay (GC)≥97.5%
It is applied In selective Suzuki coupling with arylboronic acids has been reported to give 6-arylpyrimidines.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is applied In selective Suzuki coupling with arylboronic acids has been reported to give 6-arylpyrimidines.

Solubility
Insoluble in water.

Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only

General References:

  1. Matteo Zanda, et al. Efficient and regioselective 4-amino-de-chlorination of 2,4,6-trichloropyrimidine with N-sodium carbamates.Tetrahedron Letters.,2000,41(11), 1757-1761.
  2. Cristina Zucca, et al. Regioselective solid-phase 4-amino-de-chlorination of 2,4,6-trichloropyrimidine by resin-supported N-potassium carbamates.Tetrahedron Letters.,2001,42(6), 1033-1035.
  3. Selective Suzuki coupling with arylboronic acids has been reported to give 6-arylpyrimidines: J. Heterocycl. Chem., 43, 127 (2006).