Weight | 217.87 g/mol |
---|---|
Formula | C4Cl4N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2,4,5,6-Tetrachloropyrimidine (1780-40-1)
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- Synthesis of Aryl-Substituted Pyrimidines by Site-Selective SuzukiMiyura Cross-Coupling Reactions of 2,4,5,6-Tetrachloropyrimidine (Advanced Synthesis & Catalysis, 2010)
- PROCESS FOR THE PREPARATION OF 2,4,5,6-TETRACHLOROPYRIMIDINE (1983)
- 2,4,5-TRICHLOROPYRIMIDINE AND 2,4,5,6-TETRACHLOROPYRIMIDINE (1967)
- Process for producing 2,4,5,6-tetrachloropyrimidine by way of 5,6-dichloro-2,4-dihydroxypyrimidine which was produced from the corresponding 5,6-dichloro-2,4-di(trihalomethyl)-pyrimidine and a process for producing 2,4-dihydroxypyrimidine derivatives (1985)
- ChemInform Abstract: Synthesis and Photophysical Properties of Alkynylated Pyrimidines by Site-Selective Sonogashira Reactions of 2,4,5,6-Tetrachloropyrimidine; First Synthesis of Tetraalkynyl-pyrimidines. (European Journal of Organic Chemistry, 2011)
- Process for the production of 2, 4, 5, 6-tetrachloropyrimidine (1960)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1(=C(N=C(N=C1Cl)Cl)Cl)Cl
-
InChIKeyGVBHCMNXRKOJRH-UHFFFAOYSA-N
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