| Weight | 113.204 g/mol |
|---|---|
| Formula | C7H15N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2,6-Dimethylpiperidine (504-03-0)
nanofin · nanophyn · 2,6-lupetidine
Score:
#1941 in Physics
,
#6082 in Chemistry
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- Synthesis of Silicon Nanowires and Nanofin Arrays Using Interference Lithography and Catalytic Etching (Nano Letters, 2008)
- Dynamic Nanofin Heat Sinks (Advanced Energy Materials, 2014)
- Silicon nanofin grating as a miniature chirality-distinguishing beam-splitter. (Nature Communications, 2014)
- Proton magnetic resonance studies of cyclic compoundsVI: Cis- and trans-2,6-dimethylpiperidine and cis (2,4), cis (4,6), cis (2,6)-2,4,6-trimethylpiperidine (Tetrahedron, 1968)
- Complexation of 2,6-Bis(acylamino)pyridines with Dipyridin-2-ylamine and 4,4-Dimethylpiperidine-2,6-dione (Journal of Physical Chemistry A, 2010)
- Experimental Vapor Pressures of 2-Phenylethylamine, Benzylamine, Triethylamine, and cis-2,6-Dimethylpiperidine in the Range between 0.2 Pa and 75 kPa (Journal of Chemical & Engineering Data, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - nanofin
- nanophyn
- 2,6-lupetidine
- nanofin hydrochloride
-
SMILESCC1CCCC(N1)C
-
InChIKeySDGKUVSVPIIUCF-UHFFFAOYSA-N
- Pubchem - 2,6-Dimethylpiperidine
- Wikipedia - nanofin
2,6-Dimethylpiperidines are chemical compounds with the formula C5H8(CH3)2NH. Three stereoisomers exist: the achiral (R,S)-isomer and the chiral (R,R)/(S,S) enantiomeric pair. Dimethylpiperidines are derivatives of the heterocycle piperidine, wherein two hydrogen atoms are replaced by methyl groups.
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