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2,6-dimethylpiperidine

Structure via PubChem · Public domain (PubChem)

EntityQ4596811· pop 11· linked from 6 articles

2,6-dimethylpiperidine

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Also 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.

In the Vinony graph

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 sections
Contents
  • 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.

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