Cas no 606-86-0 (1,3,3-Triphenylpropan-1-One)
1,3,3-Triphenylpropan-1-One Chemical and Physical Properties
Names and Identifiers
-
- 1-Propanone,1,3,3-triphenyl-
- 1,3,3-triphenylpropan-1-one
- 3,3-Diphenylpropiophenone
- Beta,beta-diphenylpropiophenone
- Propiophenone, 3,3-diphenyl-
- 1,3,3-Triphenylpropan-1-One
-
- Inchi: InChI=1S/C21H18O/c22-21(19-14-8-3-9-15-19)16-20(17-10-4-1-5-11-17)18-12-6-2-7-13-18/h1-15,20H,16H2
- InChI Key: WYRBITQXPQGTBL-UHFFFAOYSA-N
- SMILES: C1=CC=C(C=C1)C(CC(=O)C2=CC=CC=C2)C3=CC=CC=C3
Computed Properties
- Exact Mass: 286.13584
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 22
- Rotatable Bond Count: 5
Experimental Properties
- PSA: 17.07
1,3,3-Triphenylpropan-1-One Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | T889183-250mg |
1,3,3-Triphenylpropan-1-One |
606-86-0 | 250mg |
$ 70.00 | 2022-06-02 | ||
| TRC | T889183-500mg |
1,3,3-Triphenylpropan-1-One |
606-86-0 | 500mg |
$ 95.00 | 2022-06-02 | ||
| TRC | T889183-2.5g |
1,3,3-Triphenylpropan-1-One |
606-86-0 | 2.5g |
$ 365.00 | 2022-06-02 |
1,3,3-Triphenylpropan-1-One Related Literature
-
Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
-
Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
-
Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
-
Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
Additional information on 1,3,3-Triphenylpropan-1-One
1,3,3-Triphenylpropan-1-One (CAS 606-86-0): A Versatile Chemical Compound with Wide Applications
1,3,3-Triphenylpropan-1-One (CAS 606-86-0), also known as Triphenylacetone, is an organic compound that belongs to the class of aromatic ketones. This compound has gained significant attention in various industries due to its unique chemical properties and versatile applications. With the increasing demand for specialized chemicals in pharmaceuticals, materials science, and organic synthesis, 1,3,3-Triphenylpropan-1-One has emerged as a valuable intermediate in many chemical processes.
The molecular structure of 1,3,3-Triphenylpropan-1-One features three phenyl groups attached to a propanone backbone, giving it distinct electronic and steric properties. This configuration makes it particularly useful in asymmetric synthesis and as a building block for more complex molecules. Researchers have been exploring its potential in photocatalysis and green chemistry applications, which aligns with current trends in sustainable chemical development.
One of the most common questions about 1,3,3-Triphenylpropan-1-One is regarding its synthesis method. The compound can be prepared through various routes, including the Friedel-Crafts acylation of benzene with appropriate precursors. Modern synthetic approaches focus on improving yield and reducing environmental impact, addressing concerns about green chemistry principles and atom economy that are currently trending in chemical research.
In the pharmaceutical industry, 1,3,3-Triphenylpropan-1-One serves as a key intermediate for the synthesis of various bioactive molecules. Its structural features make it valuable for developing compounds with potential therapeutic applications, particularly in areas like central nervous system drugs and anti-inflammatory agents. These applications are especially relevant given the current global focus on healthcare innovation and drug discovery.
The material science field has also found uses for 1,3,3-Triphenylpropan-1-One, particularly in the development of advanced polymers and functional materials. Its aromatic structure contributes to thermal stability and interesting optical properties, making it suitable for applications in organic electronics and photovoltaic materials - areas that are receiving increased attention due to the growing renewable energy sector.
From a commercial perspective, the global market for 1,3,3-Triphenylpropan-1-One has been steadily growing, driven by demand from pharmaceutical and specialty chemical industries. Manufacturers are focusing on improving production processes to meet the increasing requirements for high-purity grades of this compound, especially for research and development purposes. Current market trends show particular interest in custom synthesis services and small-scale production for laboratory use.
Safety and handling of 1,3,3-Triphenylpropan-1-One are frequently searched topics. While not classified as hazardous under standard conditions, proper laboratory practices should always be followed when working with this compound. Researchers often inquire about its storage conditions, solubility characteristics, and compatibility with other reagents - information that's crucial for experimental design and process optimization.
The analytical characterization of 1,3,3-Triphenylpropan-1-One typically involves techniques such as NMR spectroscopy, mass spectrometry, and HPLC analysis. These methods are essential for quality control and verification of synthetic products, addressing common questions about compound purity assessment and structural confirmation in chemical research.
Recent scientific literature has highlighted novel applications of 1,3,3-Triphenylpropan-1-One in catalysis and materials science. Its use as a ligand in transition metal complexes and as a precursor for functional materials demonstrates the compound's versatility. These developments align with current research trends focusing on multifunctional materials and smart chemical systems.
For researchers working with 1,3,3-Triphenylpropan-1-One, understanding its reactivity patterns and derivatization possibilities is crucial. The compound participates in various organic reactions, including reductions, oxidations, and condensation reactions, making it a valuable tool in synthetic chemistry. These properties are particularly relevant to current interests in molecular diversity generation and library synthesis for drug discovery.
The future outlook for 1,3,3-Triphenylpropan-1-One appears promising, with potential applications emerging in areas like organic electronics, advanced coatings, and specialty additives. As chemical research continues to evolve toward more sophisticated and targeted applications, compounds with well-defined structures and versatile reactivity like 1,3,3-Triphenylpropan-1-One will likely maintain their importance in both academic and industrial settings.
Environmental considerations regarding 1,3,3-Triphenylpropan-1-One have also gained attention, particularly concerning its biodegradability and ecological impact. These aspects are increasingly important in chemical development, reflecting the broader societal shift toward environmentally friendly processes and sustainable chemistry practices that dominate current discussions in the field.
In conclusion, 1,3,3-Triphenylpropan-1-One (CAS 606-86-0) represents an important chemical building block with diverse applications across multiple scientific disciplines. Its unique structural features and chemical properties continue to make it valuable for researchers and industries alike, particularly in areas aligned with current scientific trends and technological advancements. As our understanding of this compound grows, so too does its potential for innovative applications in chemistry and materials science.
606-86-0 (1,3,3-Triphenylpropan-1-One) Related Products
- 1533-20-6(1,3-Diphenyl-1-butanone)
- 16282-16-9(1,2-Diphenylbutan-1-one)
- 13211-01-3(1-1,1'-Biphenyl-4-yl-1-butanone)
- 1671-77-8(4’-Methylvalerophenone)
- 37593-03-6(4'-Heptylacetophenone)
- 37593-05-8(4-n-Nonylacetophenone)
- 16819-79-7(2-Methyl-1-phenylbutan-1-one)
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)