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
製品番号(カタログ番号) A12842.22
または、製品番号A12842-22
価格(JPY)
-
数量:
100 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS3764-01-0
IUPAC Name2,4,6-trichloropyrimidine
Molecular FormulaC4HCl3N2
InChI KeyDPVIABCMTHHTGB-UHFFFAOYSA-N
SMILESClC1=CC(Cl)=NC(Cl)=N1
さらに表示
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).