coniine


coniine; α-propylpiperidine; 2-propylpiperidine
Links:🌍 Wikipedia, ⚗️ ChemSynthesis, 📖 PubMed,
📖Houben-Weyl, 2. Band (Coniin); p. 79, 206, 282, 307, 679, 732, 752, 860, 862,
CAS RN:[3238-60-6]
Formula:C8H17N; 127.23 g/mol
InChiKey:NDNUANOUGZGEPO-UHFFFAOYSA-N
SMILES:CCCC1CCCCN1
Molecular structure of coniine
Toxicology (LD50):51.0 mg/Kg (dog, sc); 16.0 mg/Kg(frog, sc); 150 mg/Kg(guinea~pig, or); 41.0 mg/Kg(guinea~pig, sc); 51.0 mg/Kg(guinea~pig, sc); 74.0 mg/Kg(mouse, sc); 16.0 mg/Kg(rabbit, iv); 57.0 mg/Kg(rabbit, or); 24.0 mg/Kg(rabbit, sc); 91.0 mg/Kg(rabbit, sc); 150 mg/Kg(rabbit, sc)
Density:0.843 g/mL
Molar volume:150.9 mL/mol
Refractive index:1.451
Molecular refractive power:40.65 mL/mol
Melting point:-2 °C
Boiling point:167 °C
1g dissolves in:
54.64g water

Isomers

azonane
Molecular structure of azonane
1-butylpyrrolidine
Molecular structure of 1-butylpyrrolidine
coniine
Molecular structure of coniine
copellidine
Molecular structure of copellidine
cycloheptanemethylamine
Molecular structure of cycloheptanemethylamine
1-cyclohexylethanamine
Molecular structure of 1-cyclohexylethanamine
2-cyclohexylethanamine
Molecular structure of 2-cyclohexylethanamine
(R)-(-)-1-cyclohexylethylamine
Molecular structure of (R)-(-)-1-cyclohexylethylamine
(S)-(+)-1-cyclohexylethylamine
Molecular structure of (S)-(+)-1-cyclohexylethylamine
cyclooctanamine
Molecular structure of cyclooctanamine
N,N-dimethylcyclohexylamine
Molecular structure of N,N-dimethylcyclohexylamine
N-ethylcyclohexylamine
Molecular structure of N-ethylcyclohexylamine
N-propylpiperidine
Molecular structure of N-propylpiperidine
(S)-2-propylpiperidine
Molecular structure of (S)-2-propylpiperidine
3-propylpiperidine
Molecular structure of 3-propylpiperidine
4-n-propylpiperidine
Molecular structure of 4-n-propylpiperidine
2,2,4-trimethylpiperidine
Molecular structure of 2,2,4-trimethylpiperidine
2α,4α,6α-trimethylpiperidine
Molecular structure of 2a,4a,6a-trimethylpiperidine