≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Reactant for synthesis of:HydrazonesSuperelectrophilic intermediates during 1,5-cyclization reactionsAmidesAnticonvulsant agentsHIV entry inhibitors for the CXCR4 receptorReactant for N-arylation reactions1-Amino-2,6-dimethylpiperidine was in the synthesis ofN-substituted derivatives of 3-aminorhodanine.
Product Application:
1-Amino-2,6-dimethylpiperidine was in the synthesis of N-substituted derivatives of 3-aminorhodanine.
Reactant for synthesis of：Hydrazones；Superelectrophilic intermediates during 1,5-cyclization reactions；Amides；Anticonvulsant agents；HIV entry inhibitors for the CXCR4 receptor；Reactant for N-arylation reactions
| Sonrisas canónicas | CC1CCCC(N1N)C |
|---|---|
| IUPAC Name | 2,6-dimethylpiperidin-1-amine |
| InChIKey | UAHWWAIVYPJROV-UHFFFAOYSA-N |
| INCHI | 1S/C7H16N2/c1-6-4-3-5-7(2)9(6)8/h6-7H,3-5,8H2,1-2H3 |
| Isómeros SMILES | CC1CCCC(N1N)C |
| WGK Alemania | 3 |
| RTECS | TM4175000 |
| Peso molecular | 128.22 |
| Reaxy-Rn | 79975 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=79975&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Piperidines |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Piperidines |
| Alternative Parents | Azacyclic compounds Alkylhydrazines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Piperidine - Alkylhydrazine - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Hydrazine derivative - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms. |
| External Descriptors | Not available |
| Índice de refracción | 1.465 |
|---|---|
| Punto de ebullición (°C) | 65-80 °C/30 mmHg |
| Peso molecular | 128.220 g/mol |
| XLogP3 | 1.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 128.131 Da |
| Monoisotopic Mass | 128.131 Da |
| Topological Polar Surface Area | 29.300 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 82.900 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
