(2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide manufacturers
- Guineensine
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- $2.00
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2026-08-25
- CAS:55038-30-7
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 100kg
- Guineesine
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- $1980.00
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2026-07-27
- CAS:55038-30-7
- Purity:
- Supply Ability: 10g
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| | (2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide Basic information |
| Product Name: | (2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide | | Synonyms: | (2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide;2,4,12-Tridecatrienamide, 13-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)-, (2E,4E,12E)-;Pipyahyine;Guineesin;Piperonal Impurity 15;(2E,4E,12E)-13-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)trideca-2,4,12-trienamide;GUINEENSINE;Guineesine | | CAS: | 55038-30-7 | | MF: | C24H33NO3 | | MW: | 383.52 | | EINECS: | | | Product Categories: | | | Mol File: | 55038-30-7.mol | ![(2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide Structure](CAS/20180601/GIF/55038-30-7.gif) |
| | (2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide Chemical Properties |
| storage temp. | -20°C | | solubility | water: slightly soluble | | form | solid | | biological source | plant | | Water Solubility | water: slightly soluble | | Major Application | metabolomics vitamins, nutraceuticals, and natural products | | InChI | 1S/C24H33NO3/c1-20(2)18-25-24(26)14-12-10-8-6-4-3-5-7-9-11-13-21-15-16-22-23(17-21)28-19-27-22/h8,10-17,20H,3-7,9,18-19H2,1-2H3,(H,25,26)/b10-8+,13-11+,14-12+ | | InChIKey | FPMPOFBEYSSYDQ-AUVZEZIHSA-N | | SMILES | N(CC(C)C)C(=O)\C=C\C=C\CCCCCC\C=C\c1cc2c(cc1)OCO2 |
| WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids |
| | (2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide Usage And Synthesis |
| Uses | It is a natural product derived from plant source th at finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research. | | Definition | ChEBI: Guineensine is a member of benzodioxoles. | | Biological Activity | According to the existing research, Guineensine inhibits endocannabinoid uptake, leading to significant anti-inflammatory and analgesic effects, and also interacts with various receptors, including dopamine transporter DAT, 5HT2A, and sigma receptors, suggesting potential polypharmacological activity. |
| | (2E,4E,12E)-13-(benzo[d][1,3]dioxol-5-yl)-N-isobutyltrideca-2,4,12-trienamide Preparation Products And Raw materials |
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