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Description générale
| Synonymes | 6-Oxabicyclo[3.1.0]hexane | AM20090363 | AKOS016042328 | 1,2- epoxycyclopentane 6-Oxabicyclo[3.1.0]hexane Cyclopentane oxide Cyclopentene epoxide Epoxycyclopentane | 6-oxa-bicyclo[3,1,0]hexane | MFCD00005161 | F0001-0897 | AKOS000121101 | NSC-196230 | cis |
|---|---|
| Spécifications et pureté | ≥97% |
| Température de stockage | Store at 2-8°C |
| Expédié en |
Wet ice Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
- Classe Oxanes
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Superclass
Organoheterocyclic compounds
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Classe | Oxanes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Oxanes |
| Alternative Parents | Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | Oxane - Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as oxanes. These are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms. |
| External Descriptors | Not available |
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Noms et identifiants
| Pubchem Sid | 488180951 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180951 |
| IUPAC Name | 6-oxabicyclo[3.1.0]hexane |
| INCHI | InChI=1S/C5H8O/c1-2-4-5(3-1)6-4/h4-5H,1-3H2 |
| InChIKey | GJEZBVHHZQAEDB-UHFFFAOYSA-N |
| Smiles | C1CC2C(C1)O2 |
| Isomères SMILES | C1CC2C(C1)O2 |
| WGK Allemagne | 3 |
| RTECS | RN8935000 |
| Numéro ONU | 1993 |
| Poids moléculaire | 84.12 |
| Beilstein | 102495 |
| Reaxy-Rn | 102495 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102495&ln= |
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 I2122126 |
Certificate of Analysis | Jul 10, 2025 | C103079 |
| I2122128 |
Certificate of Analysis | Jul 10, 2025 | C103079 |
| H2408309 |
Certificate of Analysis | Apr 02, 2024 | C103079 |
| H2310363 |
Certificate of Analysis | Jul 29, 2023 | C103079 |
| F2520027 |
Certificate of Analysis | Jul 29, 2023 | C103079 |
| H2310364 |
Certificate of Analysis | Jul 29, 2023 | C103079 |
| C2324411 |
Certificate of Analysis | Jan 03, 2023 | C103079 |
| C2324412 |
Certificate of Analysis | Jan 03, 2023 | C103079 |
| C2324405 |
Certificate of Analysis | Jan 03, 2023 | C103079 |
| C2324406 |
Certificate of Analysis | Jan 03, 2023 | C103079 |
| C2324407 |
Certificate of Analysis | Jan 03, 2023 | C103079 |
| C2324410 |
Certificate of Analysis | Jan 03, 2023 | C103079 |
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Propriétés chimiques et physiques
| Indice de réfraction | 1.434 |
|---|---|
| Point d'éclair (°F) | 10 °C |
| Point d'éclair (°C) | 10°C |
| Point d'ébullition (°C) | 102°C |
| Poids moléculaire | 84.120 g/mol |
| XLogP3 | 0.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 84.0575 Da |
| Monoisotopic Mass | 84.0575 Da |
| Topological Polar Surface Area | 12.500 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 62.300 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Citations of This Product
| 1. Wen-Wang Yu, Xiang-Guang Meng, Wen Li, Li-Yu Chen, Zi-Yu Gan, Yu-Lian Zhang, Jie Zhou. (2024) Highly efficient capture and conversion of CO2 into cyclic carbonates from actual flue gas under atmospheric pressure. Journal of Environmental Chemical Engineering, 12 (113614). |
| 2. Chi Mingfang, Ke Jingwen, Liu Yan, Wei Miaojin, Li Hongliang, Zhao Jiankang, Zhou Yuxuan, Gu Zhenhua, Geng Zhigang, Zeng Jie. (2024) Spatial decoupling of bromide-mediated process boosts propylene oxide electrosynthesis. Nature Communications, 15 (1): (1-8). |
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