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SDS
COO/COA
OMY003
Favorite1,1,7,7-tetramethyl-9-formyljulolidine
suitable for HPLC, ≥97%
Synonym(s): 1,1,7,7-Tetramethyl-2,3,6,7-tetrahydro-1h,5h-pyrido[3,2,1-ij]quinoline-9-carbaldehyde
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| Pack Size | SKU | Availability | Price | Quantity |
|---|---|---|---|---|
| 100mg | OMY003-100mg | In stock | $90.00 |
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| 250mg | OMY003-250mg | In stock | $180.00 |
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| 1g | OMY003-1g | In stock | $585.00 |
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Product Information
General Properties
Other Properties
Description
Safety Information
Product Information
| CAS Number | 216978-79-9 |
| Linear Formula |
C17H23NO |
| Molecular weight | 257.37 |
| Beilstein | |
| EC Number | |
| MDL Number | |
| PubChem CID | 22599100 |
| PubChem SID |
General Properties
| Purity | 97% |
| Appearance | light yellow solid |
| Purity Testing Method | HPLC |
| Structural Identification Method | NMR/MS |
| SMILES string | CC1(CCN2CCC(C3=C2C1=CC(=C3)C=O)(C)C)C |
Other Properties
DESCRIPTION
As a julolidine derivative, this compound exemplifies three key research themes:
- Synthetic versatility : Ruthenium-catalyzed reductive amination and hydrogenation enable efficient access to chiral derivatives.
- Electronic tunability : The aldehyde moiety serves as a reactive handle for Schiff base formation, facilitating integration into covalent organic frameworks.
- Material science applications : Its rigid, conjugated structure underpins use in:
- Organic light-emitting diodes (OLEDs).
- Fluorescent molecular rotors for viscosity sensing.
- Photopolymerizable coatings.
Recent studies highlight its role in synthesizing hexahydrojulolidines and asymmetric catalysts, underscoring its centrality in modern heterocyclic chemistry.
SAFETY INFORMATION
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Symbol GHS
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RIDADR
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WGK Germany
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RTECS
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F
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