≥98% 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.
Description
(-)-cis-Myrtanylamine may be used:As a reactant to prepareN,N-bis((-)-cis-myrtanyl)butylene-2,3-diimine (BMDI), a bidentate diimine ligand that can form transition metal complexes for catalyzing asymmetric synthesis.As a building block to prepare imidazole derivatives, which are potent and selective cannabinoid receptor (CB2) antagonists.To prepare a chiral catalyst, which can catalyze asymmetric three-component Mannich reaction.
| Pubchem Sid | 488197268 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488197268 |
| Sorrisi canonici | CC1(C)[C@@]2([H])CC[C@](CN)([H])[C@@]1(C2)[H] |
| IUPAC Name | [(1S,2R,5S)-6,6-dimethyl-2-bicyclo[3.1.1]heptanyl]methanamine |
| InChIKey | SYJBFPCQIJQYNV-CIUDSAMLSA-N |
| INCHI | 1S/C10H19N/c1-10(2)8-4-3-7(6-11)9(10)5-8/h7-9H,3-6,11H2,1-2H3/t7-,8-,9-/m0/s1 |
| Isomeri SMILES | CC1([C@H]2CC[C@H]([C@@H]1C2)CN)C |
| Numero UN | 2735 |
| Peso molecolare | 153.26 |
| Reaxy-Rn | 5239927 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5239927&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 | Lipids and lipid-like molecules |
| Classe | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Bicyclic monoterpenoids |
| Alternative Parents | Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Pinane monoterpenoid - Bicyclic monoterpenoid - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic homopolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 C2310889 | Certificate of Analysis | Jan 05, 2026 | C472607 |
| C2310888 | Certificate of Analysis | Jan 05, 2026 | C472607 |
| F2523337 | Certificate of Analysis | Nov 27, 2024 | C472607 |
| L2412463 | Certificate of Analysis | Nov 27, 2024 | C472607 |
| Indice di rifrazione | n20/D 1.4877 (lit.) |
|---|---|
| Rotazione specifica [α] | [α]22/D −30.5°, neat |
| Punto di infiammabilità (°F) | 172.4 °F - closed cup |
| Punto di infiammabilità (°C) | 78 °C - closed cup |
| Punto di ebollizione (°C) | 94-99℃/27mmHg (lit.) |
| Peso molecolare | 153.260 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 153.152 Da |
| Monoisotopic Mass | 153.152 Da |
| Topological Polar Surface Area | 26.000 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 162.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
