≥95%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504752432 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752432 |
| 정식 스마일 | C1CC=CC(C1)O |
| IUPAC Name | cyclohex-2-en-1-ol |
| InChIKey | PQANGXXSEABURG-UHFFFAOYSA-N |
| INCHI | 1S/C6H10O/c7-6-4-2-1-3-5-6/h2,4,6-7H,1,3,5H2 |
| 이성체 SMILES | C1CC=CC(C1)O |
| 분자량 | 98.15 |
| Beilstein | 6(2)60 |
| Reaxy-Rn | 5240533 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5240533&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 |
| 분류 | Organooxygen compounds |
| Subclass | Alcohols and polyols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Secondary alcohols |
| Alternative Parents | Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Secondary alcohol - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| 설명 | This compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | 날짜 | 항목 |
|---|---|---|---|
 K2421067 | Certificate of Analysis | Sep 04, 2026 | C137053 |
| K2113605 | Certificate of Analysis | May 07, 2025 | C137053 |
| K2113607 | Certificate of Analysis | May 07, 2025 | C137053 |
| K2113608 | Certificate of Analysis | May 07, 2025 | C137053 |
| K2009208 | Certificate of Analysis | Jun 05, 2024 | C137053 |
| B2006125 | Certificate of Analysis | Sep 05, 2023 | C137053 |
| 굴절률 | 1.49 |
|---|---|
| 발화점(°F) | 58°C |
| 발화점(°C) | 58°C |
| 끓는점(°C) | 166°C |
| 녹는점(°C) | 164-166°C |
| 분자량 | 98.140 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 98.0732 Da |
| Monoisotopic Mass | 98.0732 Da |
| Topological Polar Surface Area | 20.200 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 76.200 |
| 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 |
| 1. Yu-Zhen Xu, Yu-Le Wang, Yu-Dong Shan, Song-Hai Wu, Yong Liu, Xu Han. (2024) Relay Catalysis for Epoxidation of Cyclohexene by Mg–Mo Bimetallic Oxides and O2 under Solvent-Free Conditions. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.4c01558] |
| 2. Shihao Su, Guojun Lv, Jialing Shen, Fuxin Wang, Lachgar Oussama, Yan Chen, Shengnan Xu. (2025) Pickering Interfacial Tandem Catalysis of Alkenes to 1,2-Diols over Manganese Oxide Catalysts at Room Temperature. ACS Catalysis, [PMID:] [10.1021/acscatal.4c06225] |
| 3. Yu-Le Wang, Songhai Wu, Yu-Zhen Xu, Yu-Dong Shan, Yong Liu, Xu Han. (2025) Importance of surface peroxo species in the epoxidation of cyclohexene by Mo-doped TS-1 and O2 under solvent-free conditions. Catalysis Science & Technology, [PMID:] [10.1039/D5CY01095K] |
| 4. Yingxuan Zhao, Chenyang Shen, Qing Liu, Siyuan Zhao, Ruiyao Zhao, Xiangke Guo, Nianhua Xue, Luming Peng, Xuefeng Guo, Yan Zhu, Weiping Ding. (2026) Electrocatalytic oxidation or amidation of olefins by asymmetric electrolytes steering carbocation pathways. GREEN CHEMISTRY, [PMID:] [10.1039/D5GC07050C] |
