| Weight | 128.562 g/mol |
|---|---|
| Formula | C5H5ClN2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-Amino-6-chloropyridine (45644-21-1)
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- Electroorganic synthesis of 6-aminonicotinic acid from 2-amino-5-chloropyridine (Tetrahedron Letters, 2003)
- Sulfur-containing Pyridine Derivatives. XLV. Synthesis of 2-Mercapto-3-amino-6-chloropyridine Derivatives (Pharmaceutical bulletin, 1955)
- Nitrogen- and sulfur-containing heterocycles: XX. Reaction of 2-mercapto-3-amino-6-chloropyridine with chlorooxalacetic ester (Chemistry of Heterocyclic Compounds, 1971)
- Synthesis of 3-chloro-6,6-diphenyl-6,11-dihydropyrido[1?,2?:1,2]imidazo-[4,5-b]quinoline based on reaction of 2-chloromethyl-4,4-diphenyl- 4h-3,1-benzoxazine with 2-amino-5-chloropyridine (Chemistry of Heterocyclic Compounds, 2004)
- Experimental (FT-IR and FT-Raman spectra) and Theoretical (Ab initio/HF, DFT/B3LYP) Study of 2-Amino-5-Chloropyridine and 2-Amino-6-Chloropyridine (chemistry and materials research, 2015)
- Synthesis of 3-Chloro-6,6-diphenyl-6,11-dihydropyrido[1,2:1,2]imidazo [4,5-b]quinoline Based on Reaction of 2-Chloromethyl-4,4-diphenyl-4H-3,1-benzoxazine with 2-Amino-5-chloropyridine. (ChemInform, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=NC(=C1)Cl)N
-
InChIKeyOBYJTLDIQBWBHM-UHFFFAOYSA-N
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