Weight | 158.986 g/mol |
---|---|
Formula | C4H3BrN2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
5-Bromopyrimidine (4595-59-9)
5-BrPy compound
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- Copper(II) Halide Complexes of 2-Aminopyrimidines: Crystal Structures of [(2-aminopyrimidine) n CuCl2] (n=1,2) and (2-amino-5-bromopyrimidine)2CuBr2 (Journal of Coordination Chemistry, 2003)
- The Reaction of 5-Bromo- and 2-Bromopyrimidine with Organolithium Compounds. (Acta Chemica Scandinavica, 1965)
- Selective brominations in nitrobenzene. A convenient synthesis of 3-brornoquinoline, 4-bromoisoquinoline, and 4-phenyl-5-bromopyrimidine (Journal of Heterocyclic Chemistry, 1973)
- Microwave-assisted palladium-catalyzed CC coupling versus nucleophilic aromatic substitution of hydrogen (SNH) in 5-bromopyrimidine by action of bithiophene and its analogues (Tetrahedron, 2013)
- SYNTHESIS AND STRUCTURE OF (2-AMINO-5-BROMOPYRIMIDINE)BROMOCOPPER(I) (Journal of Coordination Chemistry, 1997)
- Reactions of the derivatives of 5-bromopyrimidine nucleosides with sodium azide. (Journal of Organic Chemistry, 1976)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-BrPy compound
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SMILESC1=C(C=NC=N1)Br
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InChIKeyGYCPLYCTMDTEPU-UHFFFAOYSA-N
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