Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™,≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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.
L-655,238 is a potent and selective inhibitor of FLAP (5-LO-activating protein). L-655,238 is an inhibitor of CysLT1 Receptor.
| pKa | pKa: 3.8 (Predicted) |
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| Canonical Smiles | CCCCCC(C1=CC(=CC=C1)OCC2=NC3=CC=CC=C3C=C2)O |
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| IUPAC Name | 1-[3-(quinolin-2-ylmethoxy)phenyl]hexan-1-ol |
| InChIKey | JRLOEMCOOZSCQP-UHFFFAOYSA-N |
| INCHI | 1S/C22H25NO2/c1-2-3-4-12-22(24)18-9-7-10-20(15-18)25-16-19-14-13-17-8-5-6-11-21(17)23-19/h5-11,13-15,22,24H,2-4,12,16H2,1H3 |
| Isomeric SMILES | CCCCCC(C1=CC(=CC=C1)OCC2=NC3=CC=CC=C3C=C2)O |
| Molecular Weight | 335.44 |
| Reaxy-Rn | 3558588 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3558588&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 |
| Class | Quinolines and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Quinolines and derivatives |
| Alternative Parents | Phenoxy compounds Phenol ethers Alkyl aryl ethers Pyridines and derivatives Heteroaromatic compounds Secondary alcohols Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Aromatic alcohols |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Quinoline - Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Pyridine - Heteroaromatic compound - Secondary alcohol - Ether - Azacycle - Alcohol - Aromatic alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as quinolines and derivatives. These are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. |
| External Descriptors | Not available |
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| Solubility | acidic PBS: <50 µg/ml;basic PBS: <50 µg/ml;DMF: >36 mg/ml;DMSO: >19 mg/ml;Ethanol: >70 mg/ml;PBS pH 7.2: <50 µg/ml |
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| Refractive Index | n20D1.61 (Predicted) |
| Boil Point(°C) | ~501.8° C at 760 mmHg (Predicted) |
| Melt Point(°C) | 92-93° C |
| Molecular Weight | 335.400 g/mol |
| XLogP3 | 5.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 8 |
| Exact Mass | 335.189 Da |
| Monoisotopic Mass | 335.189 Da |
| Topological Polar Surface Area | 42.400 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 375.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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