Structure via PubChem · Public domain (PubChem)
2,6-dimethylpiperidine
Sign in to saveAlso known as 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.
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.