Determine the necessary mass, volume, or concentration for preparing a solution.
≥97% 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488184926 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184926 |
| Canonical Smiles | C=CCOC1=CC=CC=C1 |
| IUPAC Name | prop-2-enoxybenzene |
| InChIKey | POSICDHOUBKJKP-UHFFFAOYSA-N |
| INCHI | 1S/C9H10O/c1-2-8-10-9-6-4-3-5-7-9/h2-7H,1,8H2 |
| Isomeric SMILES | C=CCOC1=CC=CC=C1 |
| WGK Germany | 3 |
| RTECS | DA8575000 |
| Molecular Weight | 134.18 |
| Beilstein | 1905622 |
| Reaxy-Rn | 1905622 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1905622&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 | Benzenoids |
| Class | Phenol ethers |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenol ethers |
| Alternative Parents | Phenoxy compounds Alkyl aryl ethers Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jun 09, 2026 | A101096 | |
| Certificate of Analysis | Jun 09, 2026 | A101096 | |
| Certificate of Analysis | Jun 09, 2026 | A101096 | |
| Certificate of Analysis | Apr 17, 2025 | A101096 | |
| Certificate of Analysis | Feb 25, 2025 | A101096 | |
| Certificate of Analysis | Feb 17, 2025 | A101096 | |
| Certificate of Analysis | Nov 13, 2024 | A101096 | |
| Certificate of Analysis | Nov 13, 2024 | A101096 | |
| Certificate of Analysis | Jun 14, 2024 | A101096 | |
| Certificate of Analysis | Jun 14, 2024 | A101096 | |
| Certificate of Analysis | Nov 14, 2023 | A101096 | |
| Certificate of Analysis | Sep 19, 2022 | A101096 |
| Refractive Index | 1.522 |
|---|---|
| Flash Point(°F) | 62℃ |
| Flash Point(°C) | 62℃ |
| Boil Point(°C) | 192°C |
| Molecular Weight | 134.170 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 3 |
| Exact Mass | 134.073 Da |
| Monoisotopic Mass | 134.073 Da |
| Topological Polar Surface Area | 9.200 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 92.900 |
| 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. Yingpeng Huo, Jiwen Hu, Yuanyuan Tu, Zhenzhu Huang, Shudong Lin, Yangfei Hu, Chao Feng. (2020) Platinum-Imidazolyl Schiff Base Complexes Immobilized in Periodic Mesoporous Organosilica Frameworks as Catalysts for Hydrosilylation. APPLIED ORGANOMETALLIC CHEMISTRY, 34 (8): (e5697). [PMID:] [10.1002/aoc.5697] |
| 2. Zheng Botuo, Zhong Liling, Wang Xiaoxiao, Lin Peiyao, Yang Zezhou, Bai Tianwen, Shen Hang, Zhang Huagui. (2024) Structural evolution during inverse vulcanization. Nature Communications, 15 (1): (1-17). [PMID:38951493] [10.1038/s41467-024-49374-y] |