Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
1,1'-(1,4-phenylene)bis-Ethanone can undergo oxidative C-C Bond Cleavage to synthesize an aryl carboxylic acid with an iodine catalyst . 1,1'-(1,4-phenylene)bis-Ethanone is also capable of Suzuki-Miyaura coupling.
| Pubchem Sid | 504752504 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752504 |
| Sonrisas canónicas | CC(=O)C1=CC=C(C=C1)C(=O)C |
| IUPAC Name | 1-(4-acetylphenyl)ethanone |
| InChIKey | SKBBQSLSGRSQAJ-UHFFFAOYSA-N |
| INCHI | 1S/C10H10O2/c1-7(11)9-3-5-10(6-4-9)8(2)12/h3-6H,1-2H3 |
| Isómeros SMILES | CC(=O)C1=CC=C(C=C1)C(=O)C |
| WGK Alemania | 3 |
| Peso molecular | 162.19 |
| Reaxy-Rn | 1907515 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1907515&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 | Organic oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones - Aryl ketones - Phenylketones |
| Direct Parent | Alkyl-phenylketones |
| Alternative Parents | Acetophenones Benzoyl derivatives Aryl alkyl ketones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Alkyl-phenylketone - Acetophenone - Aryl alkyl ketone - Benzoyl - Benzenoid - Monocyclic benzene moiety - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Dec 10, 2025 | D154226 | |
| Certificate of Analysis | Dec 10, 2025 | D154226 | |
| Certificate of Analysis | Jul 15, 2024 | D154226 | |
| Certificate of Analysis | Feb 23, 2024 | D154226 | |
| Certificate of Analysis | Feb 23, 2024 | D154226 | |
| Certificate of Analysis | Feb 23, 2024 | D154226 | |
| Certificate of Analysis | Feb 23, 2024 | D154226 | |
| Certificate of Analysis | Feb 23, 2024 | D154226 | |
| Certificate of Analysis | Feb 12, 2022 | D154226 | |
| Certificate of Analysis | Feb 12, 2022 | D154226 |
| Solubilidad | Solubility in hot Methanol almost transparency |
|---|---|
| Punto de ebullición (°C) | 120°C/1mmHg |
| Punto de fusión (°C) | 111-115°C |
| Peso molecular | 162.180 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 162.068 Da |
| Monoisotopic Mass | 162.068 Da |
| Topological Polar Surface Area | 34.100 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 166.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 |
| 1. Qianwen Su, Yinying Wang, Jinghao Chen, Daohui Zhao, Huali Long, Ming Li. (2022) Ultrafast organic solvent nanofiltration in CC bonded conjugated microporous membrane-based nanochannels by space-confined polymerization. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2022.141130] |
| 2. Ren Jing, Tang Jing, Zhao Mei, Chen Zilin, Wang Fang. (2024) Enhanced electrochemical sensing of uracil via a glassy carbon electrode modified with a COF-V-AuNP composite. JOURNAL OF SOLID STATE ELECTROCHEMISTRY, [PMID:] [10.1007/s10008-024-05942-2] |
| 3. Qi Zhou, Lijiang Guan, Mohamed E. El-Khouly, Shangbin Jin. (2025) Synthesis of Pyrrole-based Porous Organic Polymers for High Temperature Proton Conduction. ACS Omega, [PMID:40821569] [10.1021/acsomega.5c00303] |
| 4. Yu Shi-Han, Wang Lu, Zhang Meng-Chao, Li Hong-Kun. (2025) Multicomponent Polymerization of Diacetylarenes, Dialkynones, and NH4OAc for In situ Construction of Functional Conjugated Poly(triarylpyridine)s. CHINESE JOURNAL OF POLYMER SCIENCE, [PMID:] [10.1007/s10118-025-3362-2] |
| 5. Min Sun, Jiaqing Feng, Yang Feng, Xubo Xin, Yali Ding, Juanjuan Feng. (2024) Core-shell silica@pyridyl conjugated microporous polymer as a stationary phase for high performance liquid chromatography. ANALYTICA CHIMICA ACTA, [PMID:38309855] [10.1016/j.aca.2024.342258] |