Weight | 173.013 g/mol |
---|---|
Formula | C5H5BrN2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
3-Amino-2-bromopyridine (39856-58-1)
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- Electrocatalytic carboxylation of 2-amino-5-bromopyridine with CO2 in ionic liquid 1-butyl-3-methyllimidazoliumtetrafluoborate to 6-aminonicotinic acid (Electrochimica Acta, 2010)
- Molecular structure and vibrational spectra of 3-and 4-amino-2-bromopyridine by density functional methods (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- 2-amino-3-iodo-5-bromopyridine method (2014)
- Synthesis of -d-glucopyranosyl- and -d-galactopyranosylamines from 4-bromo-3-methylaniline and 2-amino-5-bromopyridine (Russian Chemical Bulletin, 2008)
- Preparation of Combinatorial Libraries of Novel Condensed Heterocycles on the Basis of 2Amino5bromopyridine3sulfonylchloride. (ChemInform, 2005)
- A new supramolecular cocrystal of 2-amino-3-bromopyridine with 4-methylbenzoic acid: Synthesis, structural, spectroscopic characterization and comparative theoretical studies (Molecular Crystals and Liquid Crystals, 2016)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(N=C1)Br)N
-
InChIKeyHKDVVTLISGIPFE-UHFFFAOYSA-N
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