Structure via PubChem · Public domain (PubChem)
2,6-dimethylpiperidine
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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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Within Vinony's link graph, 2,6-dimethylpiperidine is referenced by 6 other articles, and connects out to chemical compound, mass density and chemical formula.
Vinony files it under Chembox having GHS data, Chemical articles with multiple compound IDs and ECHA InfoCard ID from Wikidata.
Its subject is documented across 10 Wikipedia language editions.
Chemical data
- Formula
- C7H15N
- Molecular weight
- 113.2 g/mol
- IUPAC name
- 2,6-dimethylpiperidine
- SMILES
- CC1CCCC(N1)C
- InChIKey
- SDGKUVSVPIIUCF-UHFFFAOYSA-N
- XLogP
- 1.5
- Polar surface area
- 12 Ų
- H-bond donors
- 1
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Has part
- hydrogen
- Mass
- 113.12
Show 4 more facts
- Commons category
- 2,6-Dimethylpiperidine
- has characteristic
- bitterness
- canonical SMILES
- CC1CCCC(N1)C
- chemical formula
- C₇H₁₅N
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- References
- See also
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.
The 2,6-dimethylpiperidines are prepared by reduction of 2,6-dimethylpyridine (2,6-lutidine). The achiral isomer is the predominant isomer produced in this reaction.
Excerpted from Wikipedia’s “2,6-dimethylpiperidine” article, available under the CC BY-SA 4.0 licence.