Search
項目搜尋
結構搜尋
Thermo Scientific Chemicals
2-Amino-4-chloropyrimidine, 98%
CAS: 3993-78-0 | C4H4ClN3 | 129.547 g/mol
Have Questions?
變更視圖
化學識別
CAS3993-78-0
IUPAC Name4-chloropyrimidin-2-amine
Molecular FormulaC4H4ClN3
InChI KeyDBGFGNCFYUNXLD-UHFFFAOYSA-N
SMILESNC1=NC=CC(Cl)=N1
檢視更多
規格
規格表
規格表Assay (HPLC)>97.5%
2-Amino-4-chloropyrimidine is a substrate used in a palladium-catalyzed cyanation with zinc(II) cyanide. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
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
2-Amino-4-chloropyrimidine is a substrate used in a palladium-catalyzed cyanation with zinc(II) cyanide. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in dimethyl sulfoxide.
Notes
Keep container tightly sealed. Store in refrigerated conditions. Incompatible with oxidizing agents and acids.
2-Amino-4-chloropyrimidine is a substrate used in a palladium-catalyzed cyanation with zinc(II) cyanide. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in dimethyl sulfoxide.
Notes
Keep container tightly sealed. Store in refrigerated conditions. Incompatible with oxidizing agents and acids.
RUO – Research Use Only
General References:
- Adam Littke.; Maxime Soumeillant.; Robert F Kaltenbach Iii.; Robert J Cherney.; Christine M Tarby.; Susanne Kiau. Mild and general methods for the palladium-catalyzed cyanation of aryl and heteroaryl chlorides. Chemical Communications. 2007, 9 (9), 1711-1714.
- C. Kenneth Banks. Arylaminoheterocyclic Compounds. I. Synthetic Method. J. Am. Chem. Soc. 1944, 66 (7), 1127-1130.