Cas no 1666-96-2 (Quinoline, 3-phenyl-)
Quinoline, 3-phenyl- Chemical and Physical Properties
Names and Identifiers
-
- Quinoline, 3-phenyl-
- 3-phenylquinoline
- 3-Phenyl-chinolin
- 3-phenyl-quinoline
- Quinoline,3-phenyl
- SB69525
- CHEMBL3805672
- DTXSID60300417
- NSC136922
- NSC-136922
- 1666-96-2
- ZPKRDBXIPFYPTF-UHFFFAOYSA-N
- BDBM50171042
- SCHEMBL708999
- EN300-7537395
- BAA66696
- NSC 136922
-
- Inchi: 1S/C15H11N/c1-2-6-12(7-3-1)14-10-13-8-4-5-9-15(13)16-11-14/h1-11H
- InChI Key: ZPKRDBXIPFYPTF-UHFFFAOYSA-N
- SMILES: C1C=CC(C2C=C3C(C=CC=C3)=NC=2)=CC=1
Computed Properties
- Exact Mass: 205.08900
- Monoisotopic Mass: 205.089149355g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 16
- Rotatable Bond Count: 1
- Complexity: 220
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.8
- Topological Polar Surface Area: 12.9?2
Experimental Properties
- PSA: 12.89000
- LogP: 3.90180
Quinoline, 3-phenyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM228625-1g |
3-Phenylquinoline |
1666-96-2 | 95% | 1g |
$449 | 2021-08-04 | |
| Chemenu | CM228625-1g |
3-Phenylquinoline |
1666-96-2 | 95% | 1g |
$475 | 2023-01-02 | |
| Enamine | EN300-7537395-0.05g |
3-phenylquinoline |
1666-96-2 | 95% | 0.05g |
$1140.0 | 2024-05-23 | |
| Enamine | EN300-7537395-0.1g |
3-phenylquinoline |
1666-96-2 | 95% | 0.1g |
$1195.0 | 2024-05-23 | |
| Enamine | EN300-7537395-0.25g |
3-phenylquinoline |
1666-96-2 | 95% | 0.25g |
$1249.0 | 2024-05-23 | |
| Enamine | EN300-7537395-0.5g |
3-phenylquinoline |
1666-96-2 | 95% | 0.5g |
$1302.0 | 2024-05-23 | |
| Enamine | EN300-7537395-1.0g |
3-phenylquinoline |
1666-96-2 | 95% | 1.0g |
$1357.0 | 2024-05-23 | |
| Enamine | EN300-7537395-2.5g |
3-phenylquinoline |
1666-96-2 | 95% | 2.5g |
$2660.0 | 2024-05-23 | |
| Enamine | EN300-7537395-5.0g |
3-phenylquinoline |
1666-96-2 | 95% | 5.0g |
$3935.0 | 2024-05-23 | |
| Enamine | EN300-7537395-10.0g |
3-phenylquinoline |
1666-96-2 | 95% | 10.0g |
$5837.0 | 2024-05-23 |
Quinoline, 3-phenyl- Related Literature
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1. 634. Some 4-(dialkylaminoalkylamino)-3-phenylquinolinesW. J. Adams,D. H. Hey J. Chem. Soc. 1950 3254
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Nicolai A. Aksenov,Alexander V. Aksenov,Nikita K. Kirilov,Nikolai A. Arutiunov,Dmitrii A. Aksenov,Vladimir Maslivetc,Zhenze Zhao,Liqin Du,Michael Rubin,Alexander Kornienko Org. Biomol. Chem. 2020 18 6651
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3. 158. Rearrangements in the oxidation of 3-phenylquinolinesC. W. Rees,C. R. Sabet J. Chem. Soc. 1965 870
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Takenori Mitamura,Kimiyo Iwata,Akihiro Nomoto,Akiya Ogawa Org. Biomol. Chem. 2011 9 3768
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5. 349. Nitrosoacylarylamines. Part V. The nitrosation of 3-acetamido-4-quinolones and -quinaldonesW. J. Adams,D. H. Hey J. Chem. Soc. 1951 1521
Additional information on Quinoline, 3-phenyl-
Comprehensive Guide to Quinoline, 3-phenyl- (CAS No. 1666-96-2): Properties, Applications, and Market Insights
Quinoline, 3-phenyl- (CAS No. 1666-96-2) is a specialized organic compound that belongs to the quinoline derivatives family. This compound is widely recognized for its unique chemical structure, combining a quinoline core with a phenyl substituent at the 3-position. Its molecular formula is C15H11N, and it exhibits notable properties such as fluorescence and aromaticity, making it valuable in various industrial and research applications.
The growing interest in Quinoline, 3-phenyl- is driven by its versatility in pharmaceutical intermediates, material science, and organic synthesis. Researchers and manufacturers frequently search for "Quinoline derivatives uses" or "CAS 1666-96-2 supplier" to explore its potential. Its role in developing fluorescent dyes and electronic materials has also gained attention, aligning with trends in sustainable technology and advanced materials.
One of the key features of Quinoline, 3-phenyl- is its stability under standard conditions, which facilitates handling and storage. The compound's melting point and solubility in organic solvents like ethanol and dimethyl sulfoxide (DMSO) are critical parameters for laboratory and industrial processes. These properties are often queried in searches such as "3-phenylquinoline solubility" or "thermal stability of quinoline derivatives."
In the pharmaceutical industry, Quinoline, 3-phenyl- serves as a building block for synthesizing bioactive molecules. Its structural motif is found in compounds with potential antimicrobial and antitumor activities, sparking interest in "quinoline-based drug discovery." Additionally, its application in OLEDs (Organic Light-Emitting Diodes) and sensors highlights its relevance in cutting-edge technologies.
The market for Quinoline, 3-phenyl- is expanding, with increasing demand from Asia-Pacific and North America. Suppliers and distributors often optimize their content for keywords like "buy 3-phenylquinoline" or "CAS 1666-96-2 price" to attract global buyers. Regulatory compliance, such as REACH and FDA guidelines, further influences its commercial availability.
Environmental and safety considerations are also pivotal. While Quinoline, 3-phenyl- is not classified as hazardous under standard regulations, proper handling protocols are recommended. Searches like "3-phenylquinoline safety data sheet" reflect user concerns about workplace safety and environmental impact.
In summary, Quinoline, 3-phenyl- (CAS No. 1666-96-2) is a multifaceted compound with significant applications across industries. Its chemical properties, coupled with emerging trends in green chemistry and high-performance materials, ensure its continued relevance. For researchers and businesses, understanding its synthesis, applications, and market dynamics is essential to leveraging its full potential.
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