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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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A101037-5ml
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5ml |
4
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$12.90
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A101037-25ml
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25ml |
Available within 1-2 weeks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
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$48.90
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A101037-100ml
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100ml |
4
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$129.90
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A101037-500ml
|
500ml |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$581.90
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| Synonyms | 3-Phenyl-1-propene | FD14063 | UNII-3VT7C9MEQ9 | Benzene, 2-propenyl- | F0001-0925 | (prop-2-en-1-yl)benzene | STL268883 | 2-Propen-1-yl-benzene | Benzene, 2-propen-1-yl- | 3VT7C9MEQ9 | EINECS 206-095-7 | DTXSID00861855 | NSC18609 | NSC-18609 | Allylbenze |
|---|---|
| Specifications & Purity | ≥98% |
| Shipped In | Normal |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzene and substituted derivatives |
| Alternative Parents | Aromatic hydrocarbons Cyclic olefins |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Monocyclic benzene moiety - Aromatic hydrocarbon - Cyclic olefin - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. |
| External Descriptors | Not available |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| Pubchem Sid | 488180966 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180966 |
| IUPAC Name | prop-2-enylbenzene |
| INCHI | InChI=1S/C9H10/c1-2-6-9-7-4-3-5-8-9/h2-5,7-8H,1,6H2 |
| InChIKey | HJWLCRVIBGQPNF-UHFFFAOYSA-N |
| Smiles | C=CCC1=CC=CC=C1 |
| Isomeric SMILES | C=CCC1=CC=CC=C1 |
| WGK Germany | 3 |
| RTECS | CY2275000 |
| UN Number | 3295 |
| Molecular Weight | 118.18 |
| Beilstein | 1098501 |
| Reaxy-Rn | 1098501 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098501&ln= |
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 17, 2025 | A101037 | |
| Certificate of Analysis | Apr 17, 2025 | A101037 | |
| Certificate of Analysis | Mar 03, 2025 | A101037 | |
| Certificate of Analysis | Mar 03, 2025 | A101037 | |
| Certificate of Analysis | Feb 07, 2025 | A101037 | |
| Certificate of Analysis | Apr 10, 2024 | A101037 | |
| Certificate of Analysis | Mar 25, 2024 | A101037 | |
| Certificate of Analysis | Mar 25, 2024 | A101037 | |
| Certificate of Analysis | Mar 25, 2024 | A101037 | |
| Certificate of Analysis | May 27, 2023 | A101037 | |
| Certificate of Analysis | May 10, 2023 | A101037 | |
| Certificate of Analysis | Feb 25, 2023 | A101037 | |
| Certificate of Analysis | Feb 25, 2023 | A101037 | |
| Certificate of Analysis | Jan 16, 2023 | A101037 | |
| Certificate of Analysis | Dec 08, 2021 | A101037 | |
| Certificate of Analysis | Dec 08, 2021 | A101037 |
| Refractive Index | 1.511 |
|---|---|
| Flash Point(°F) | 92 °F |
| Flash Point(°C) | 33℃ |
| Boil Point(°C) | 156-157°C |
| Melt Point(°C) | 557 °C |
| Molecular Weight | 118.180 g/mol |
| XLogP3 | 3.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 118.078 Da |
| Monoisotopic Mass | 118.078 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 78.000 |
| 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. Dong Li, Kaixuan Wang, Jiahong Tang, Yizhou Zhao, Hanan Elhaes, Muhammad Tahir, Medhat A. Ibrahim, Yujing Li. (2023) Efficient photosensitized singlet oxygen generation in two-dimensional perovskite nanosheets via energy transfer. APPLIED SURFACE SCIENCE, 613 (155991). |
| 2. Dingxuan Ma, Yaowen Zhang, Huihui Zhao, Kang Liu, Lei Wang. (2022) Directing two copper porphyrin based polymers as highly efficient heterogeneous catalysts for styrene oxidation. APPLIED SURFACE SCIENCE, 571 (151363). |
| 3. Gaoyi Yi, Jingxia He, Baian Ji, Die Gao, Kailian Zhang, Lujun Wang, Jing Zeng, Zhining Xia, Qifeng Fu. (2020) Solvothermal-assisted in situ rapid growth of octadecylamine functionalized polydopamine-based permanent coating as stationary phase for open-tubular capillary electrochromatography. JOURNAL OF CHROMATOGRAPHY A, 1628 (461436). |
| 4. 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). |
| 5. Hui Lin, Yanhong Tang, Shuang Dong, Ruibo Lang, Hongge Chen. (2020) A new monooxygenase from Herbaspirillum huttiense catalyzed highly enantioselective epoxidation of allylbenzenes and allylic alcohols. Catalysis Science & Technology, 10 (7): (2145-2151). |
| 6. Xueping Tao, Mengting Su, Panpan Chen, Meiting Yan, Dan Wang, Lan Xia, Li Rao, Zhining Xia, Qifeng Fu. (2024) Zirconium(IV) coordination-mediated rapid and versatile post-modification of polydopamine coating as stationary phase for open-tubular capillary electrochromatography. JOURNAL OF CHROMATOGRAPHY A, 1736 (465415). |