Cas no 15051-81-7 (epi-Eudesmol)
epi-Eudesmol Chemical and Physical Properties
Names and Identifiers
-
- 2-Naphthalenemethanol,1,2,3,4,4a,5,6,7-octahydro-a,a,4a,8-tetramethyl-, (2R,4aS)-
- 2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-ol
- epi-Eudesmol
- γ
- epi-10- γ
- -Eudesmol
- -Eudesmol, 10-epi-
- [ "" ]
- 10-epi-γ-eudesmol
- AKOS032948531
- WMOPMQRJLLIEJV-DOMZBBRYSA-N
- (2R-trans)-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol
- 2-[(2R,4aS)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl]propan-2-ol
- FS-10402
- (-)-10-epi- .gamma.-eudesmol
- A-eudesmol
- 10-Eudesm-4-en-11-ol
- 10-epi-
- 2-((2R,4AS)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-ol
- 15051-81-7
- epi-10- .gamma.-Eudesmol
- Q27131975
- 10-epi-eudesm-4-en-11-ol
- 2-Naphthalenemethanol, 1,2,3,4,4a,5,6,7-octahydro-alpha,alpha,4a,8-tetramethyl-, (2R-trans)-
- (-)-10-epi--Eudesmol; 10-epi--Eudesmol; epi-Eudesmol
- C19893
- CHEBI:62514
- 10-epi-gamma-Eudesmol
- SCHEMBL310948
- 10alpha-Eudesm-4-en-11-ol
- 10a-Eudesm-4-en-11-ol
- 2-((2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)propan-2-ol
- 10-epi-eudesm-4-en-11-ol;2-((2R,4aS)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-ol
- 10-Epi-I3-eudesmol
- 10-epi-eudesm-4-en-11-ol;2-[(2R,4aS)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl]propan-2-ol
- 10-Epi-g-eudesmol
-
- Inchi： 1S/C15H26O/c1-11-6-5-8-15(4)9-7-12(10-13(11)15)14(2,3)16/h12,16H,5-10H2,1-4H3/t12-,15+/m1/s1
- InChI Key： WMOPMQRJLLIEJV-DOMZBBRYSA-N
- SMILES： OC(C)(C)[C@@H]1CC[C@]2(C)CCCC(C)=C2C1
Computed Properties
- Exact Mass: 222.198365449g/mol
- Monoisotopic Mass: 222.198365449g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 16
- Rotatable Bond Count: 1
- Complexity: 313
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 2
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.4
- Topological Polar Surface Area: 20.2?2
Experimental Properties
- Color/Form: Oil
epi-Eudesmol Security Information
- Hazard Statement： H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement： P264+P280+P305+P351+P338+P337+P313
- Safety Instruction： H303+H313+H333
- Storage Condition：Store at 4 ℃, better at -4 ℃
epi-Eudesmol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | E34680-5mg |
2-Naphthalenemethanol,1,2,3,4,4a,5,6,7-octahydro-a,a,4a,8-tetramethyl-, (2R,4aS)- |
15051-81-7 | ,GC≥98% | 5mg |
￥4002.0 | 2023-09-08 | |
| TRC | E582620-2.5mg |
epi-Eudesmol |
15051-81-7 | 2.5mg |
$184.00 | 2023-05-18 | ||
| TRC | E582620-10mg |
epi-Eudesmol |
15051-81-7 | 10mg |
$695.00 | 2023-05-18 | ||
| TRC | E582620-25mg |
epi-Eudesmol |
15051-81-7 | 25mg |
$1447.00 | 2023-05-18 | ||
| TRC | E582620-100mg |
epi-Eudesmol |
15051-81-7 | 100mg |
$ 4500.00 | 2023-09-07 | ||
| TargetMol Chemicals | TN3962-5 mg |
epi-Eudesmol |
15051-81-7 | 98% | 5mg |
￥ 3,040 | 2023-07-10 | |
| TargetMol Chemicals | TN3962-1 mL * 10 mM (in DMSO) |
epi-Eudesmol |
15051-81-7 | 98% | 1 mL * 10 mM (in DMSO) |
￥ 3140 | 2023-09-15 | |
| TargetMol Chemicals | TN3962-5mg |
epi-Eudesmol |
15051-81-7 | 5mg |
￥ 3040 | 2024-07-19 | ||
| A2B Chem LLC | AE93469-1mg |
10-epi-γ-eudesmol |
15051-81-7 | 95% | 1mg |
$246.00 | 2024-04-20 | |
| TargetMol Chemicals | TN3962-1 ml * 10 mm |
epi-Eudesmol |
15051-81-7 | 1 ml * 10 mm |
￥ 3140 | 2024-07-19 |
epi-Eudesmol Related Literature
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
-
Kui Wu,Zhihua Yang,Shilie Pan Dalton Trans., 2015,44, 19856-19864
-
Raktani Bikshapathi,Sai Prathima Parvathaneni,Vaidya Jayathirtha Rao Green Chem., 2017,19, 4446-4450
-
Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
Related Categories
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
- Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Prenol lipids Sesquiterpenoids Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Additional information on epi-Eudesmol
Epi-Eudesmol: A Comprehensive Overview
Epi-eudesmol, also known by its CAS number 15051-81-7, is a naturally occurring sesquiterpene that has garnered significant attention in recent years due to its diverse biological activities and applications. This compound is primarily found in various plant species, particularly in the essential oils of certain aromatic plants. Epi-eudesmol has been extensively studied for its potential in the fields of medicine, food additives, and cosmetics. This article delves into the latest research findings, structural properties, and applications of epi-eudesmol.
Structural Insights and Synthesis
Epi-eudesmol belongs to the class of sesquiterpenes, which are a group of terpenoid compounds composed of 15 carbon atoms. Its structure is characterized by a bicyclic framework with a specific arrangement of methyl groups and double bonds. The compound exhibits a unique stereochemistry, which plays a crucial role in its biological activities. Recent advancements in synthetic chemistry have enabled researchers to develop efficient methods for the synthesis of epi-eudesmol, making it more accessible for large-scale applications.
Biological Activities and Applications
Epi-eudesmol has been reported to possess a wide range of biological activities, including antimicrobial, anti-inflammatory, and antioxidant properties. A study published in 2023 highlighted its potential as an effective natural preservative in food products due to its ability to inhibit the growth of pathogenic bacteria. Additionally, epi-eudesmol has shown promising results in reducing inflammation in experimental models, suggesting its potential use in treating inflammatory diseases.
Pharmacological Studies
Recent pharmacological studies have focused on the mechanism of action of epi-eudesmol. Researchers have identified that the compound interacts with key cellular pathways involved in inflammation and oxidative stress. For instance, epi-eudesmol has been found to modulate the NF-kB pathway, which is central to inflammatory responses. These findings underscore its potential as a therapeutic agent in conditions such as arthritis and neurodegenerative diseases.
Safety and Toxicology
The safety profile of epi-eudesmol is another critical aspect that has been extensively investigated. According to recent toxicological studies, epi-eudesmol exhibits low toxicity at therapeutic doses, making it suitable for use in both food and pharmaceutical applications. However, further studies are required to fully understand its long-term effects and potential interactions with other compounds.
Future Directions and Market Potential
The growing demand for natural products in various industries presents a significant opportunity for epi-eudesmol. With its versatile properties and increasing scientific backing, epi-eudesmol is poised to become a key ingredient in functional foods, cosmetics, and pharmaceuticals. Ongoing research is focused on optimizing its extraction methods and exploring new applications to meet the demands of a global market.
In conclusion, epi-eudesmol (CAS No 15051-81-7) is a multifaceted compound with immense potential across multiple sectors. Its unique chemical structure, coupled with its diverse biological activities, makes it an intriguing subject for further research and development. As scientific understanding of this compound continues to evolve, it is likely to play an increasingly important role in both traditional and modern applications.
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