| Weight | 113.547 g/mol |
|---|---|
| Formula | C5H4ClN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-CHLOROPYRIDINE (626-60-8)
Score:
#2335 in Physics
,
#7172 in Chemistry
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- Synthesis and Structural Characterization of the One-Dimensional [Cu(3-Clpy)(2)(N(3))(2)](n)() Complex (3-Clpy = 3-Chloropyridine): A Singular Ferrimagnetic Chain with Local S(A) = S(B). (Inorganic Chemistry, 1998)
- Structural characterization of a variable-spin(porphinato)iron(III) complex. Molecular stereochemistry of bis(3-chloropyridine)(octaethylporphinato)iron(III) perchlorate at 98 K (S = 1/2) and 293 K (S = 1/2, S = 5/2) (Journal of the American Chemical Society, 1982)
- Control of spin state in (porphinato)iron(III) complexes. An axial ligand orientation effect leading to an intermediate-spin complex. Molecular structure and physical characterization of the monoclinic form of bis(3-chloropyridine)(octaethylporphinato)iron(III) perchlorate (Journal of the American Chemical Society, 1983)
- Improved synthesis of 2,3-disubstituted pyridines by metallation of 2-chloropyridine: a convenient route to fused polyheterocycles (Journal of The Chemical Society-perkin Transactions 1, 1990)
- A comparative study of photocatalytic degradation of 3-chloropyridine under UV and solar light by homogeneous (photo-Fenton) and heterogeneous (TiO2) photocatalysis (Applied Catalysis B-environmental, 2012)
- Multipotent drugs with cholinergic and neuroprotective properties for the treatment of Alzheimer and neuronal vascular diseases. I. Synthesis, biological assessment, and molecular modeling of simple and readily available 2-aminopyridine-, and 2-chloropyridine-3,5-dicarbonitriles. (Bioorganic & Medicinal Chemistry, 2010)
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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(=CN=C1)Cl
-
InChIKeyPWRBCZZQRRPXAB-UHFFFAOYSA-N
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8-chloroisoquinoline
(34784-07-1)
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3-CHLOROPYRIDINE
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