Cas no 6380-28-5 (Carvacryl acetate)
Carvacryl acetate Chemical and Physical Properties
Names and Identifiers
-
- Carvacryl acetate
- 5-Isopropyl-o-tolyl acetate
- 5-Isopropyl-2-methylphenyl acetate
- CARVACRYL ACETATE(RG)
- ACETIC ACID 5-ISOPROPYL-2-METHYL-PHENYL ESTER
- carvacrol acetate
- Essigsaeure-(5-isopropyl-2-methyl-phenylester)
- Essigsaeure-carvacrylester
- O-acetylcarvacrol
- Phenol,2-methyl-5-(1-methylethyl)-,acetate
- 5-Isopropyl-2-methylphenyl acetate #
- OXZSUQJHKQOGOK-UHFFFAOYSA-N
- AKOS006227942
- NSC 6601
- NS00044622
- DTXSID40863777
- Acetic acid, carvacryl-,
- UNII-2A2BR75B36
- SCHEMBL247416
- (2-methyl-5-propan-2-ylphenyl) acetate
- 5-Isopropyl-2-methylphenol acetate
- MFCD00270428
- 4395-82-8
- CHEBI:179898
- AI3-03429
- 2A2BR75B36
- Q27254462
- 2-methyl-5-(propan-2-yl)phenyl acetate
- NSC-6601
- Acetic acid, carvacryl-
- Phenol, 2-methyl-5-(1-methylethyl)-, acetate
- NSC6601
- EINECS 228-963-4
- 6380-28-5
-
- MDL： MFCD00270428
- Inchi： 1S/C12H16O2/c1-8(2)11-6-5-9(3)12(7-11)14-10(4)13/h5-8H,1-4H3
- InChI Key： OXZSUQJHKQOGOK-UHFFFAOYSA-N
- SMILES： O(C(C)=O)C1=C(C)C=CC(=C1)C(C)C
Computed Properties
- Exact Mass: 192.11500
- Monoisotopic Mass: 192.115029749g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 14
- Rotatable Bond Count: 3
- Complexity: 199
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 26.3?2
Experimental Properties
- Density: 0.9896
- Boiling Point: 246.5°C (estimate)
- Refractive Index: 1.4913 (estimate)
- PSA: 26.30000
- LogP: 3.04370
Carvacryl acetate Customs Data
- HS CODE：2915390090
- Customs Data：
China Customs Code:
2915390090Overview:
2915390090. Other acetate esters. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Regulatory conditions:
A.Customs clearance form for Inbound Goods
B.Customs clearance form for outbound goodsInspection and quarantine category:
R.Sanitary supervision and inspection of imported food
S.Sanitary supervision and inspection of exported food
M.Import commodity inspection
N.Export commodity inspectionSummary:
2915390090. esters of acetic acid. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:5.5%. General tariff:30.0%
Carvacryl acetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB165485-1 g |
Carvacryl acetate |
6380-28-5 | 1 g |
€112.00 | 2023-07-20 | ||
| abcr | AB165485-5 g |
Carvacryl acetate |
6380-28-5 | 5 g |
€340.00 | 2023-07-20 | ||
| abcr | AB165485-10 g |
Carvacryl acetate |
6380-28-5 | 10 g |
€625.00 | 2023-07-20 | ||
| abcr | AB165485-1g |
Carvacryl acetate; . |
6380-28-5 | 1g |
€112.00 | 2025-04-17 | ||
| abcr | AB165485-5g |
Carvacryl acetate; . |
6380-28-5 | 5g |
€340.00 | 2025-04-17 | ||
| abcr | AB165485-10g |
Carvacryl acetate; . |
6380-28-5 | 10g |
€625.00 | 2025-04-17 |
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Carvacryl acetate Related Literature
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Ying Song,Li-Bo Wang,Yun Bei,Dong-Xu Qin,Li-Yao Ai,Qi-Zhuang Ma,Pei-Yao Lin Food Funct. 2020 11 1754
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2. 837. Further rearrangements of eucarvone derivativesG. L. Buchanan,R. A. Raphael,I. W. J. Still J. Chem. Soc. 1963 4372
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Nitin Tandon,Shripad M. Patil,Runjhun Tandon,Pushpendra Kumar RSC Adv. 2021 11 21291
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Na Yang,Han Wang,Hongqiang Lin,Junli Liu,Baisong Zhou,Xiaoling Chen,Cuizhu Wang,Jinping Liu,Pingya Li RSC Adv. 2020 10 8396
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Nan Shen,Wen Zeng,Feng Leng,Jinkai Lu,Zhaogeng Lu,Jiawen Cui,Li Wang,Biao Jin Food Funct. 2021 12 12395
Additional information on Carvacryl acetate
Carvacryl acetate (CAS No. 6380-28-5): A Comprehensive Overview
Carvacryl acetate, with the chemical formula C10H10O2 and CAS number 6380-28-5, is a versatile organic compound that has garnered significant attention in the field of pharmaceuticals, agrochemicals, and specialty chemicals. This ester derivative of carvone exhibits a range of biological activities and industrial applications, making it a subject of extensive research and development.
The compound is primarily known for its role as an intermediate in the synthesis of various pharmaceuticals and fragrances. Its unique structural properties, characterized by a carbonyl group and a substituted phenyl ring, contribute to its reactivity and functional versatility. In recent years, Carvacryl acetate has been explored for its potential in drug development, particularly in the treatment of inflammatory diseases and microbial infections.
One of the most compelling aspects of Carvacryl acetate is its biological activity. Studies have demonstrated its efficacy as an anti-inflammatory agent, with mechanisms that involve the modulation of cytokine production and inhibition of pro-inflammatory enzymes. This has led to its investigation as a potential therapeutic agent in conditions such as rheumatoid arthritis and inflammatory bowel disease. Additionally, research has highlighted its antimicrobial properties, making it a promising candidate for developing novel antibiotics and antifungal agents.
The chemical structure of Carvacryl acetate (CAS No. 6380-28-5) allows for diverse chemical modifications, which has opened up avenues for synthetic chemists to develop derivatives with enhanced pharmacological properties. For instance, modifications at the phenyl ring or the ester group can lead to compounds with improved bioavailability or targeted action. These structural variations are being actively studied to optimize drug candidates for clinical use.
In the realm of agrochemicals, Carvacryl acetate has shown promise as a natural pesticide due to its ability to repel certain insects while being less toxic to non-target organisms. This aligns with the growing demand for environmentally friendly agricultural practices. Researchers are exploring its potential as a component in bio-based pest control formulations, which could reduce reliance on synthetic pesticides and minimize ecological impact.
The industrial applications of Carvacryl acetate extend beyond pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of fragrances and flavoring agents, where its aromatic properties contribute to desirable sensory experiences in consumer products. Furthermore, its stability under various conditions makes it suitable for use in coatings and adhesives, where chemical resistance is crucial.
The synthesis of Carvacryl acetate (CAS No. 6380-28-5) typically involves the esterification of carvone with acetic acid under controlled conditions. Advances in catalytic processes have improved the efficiency and yield of this reaction, making it more sustainable and cost-effective. These innovations are essential for meeting the increasing demand for high-purity Carvacryl acetate in industrial applications.
Ongoing research into Carvacryl acetate continues to uncover new possibilities for its use in medicine and industry. For example, studies are exploring its potential role in photodynamic therapy due to its ability to generate reactive oxygen species when exposed to light. This could open up new avenues for treating cancer and other degenerative diseases.
The regulatory landscape surrounding the use of Carvacryl acetate is also evolving, with increasing emphasis on safety and environmental impact assessments. Regulatory bodies are keen on ensuring that products containing this compound meet stringent standards to protect human health and ecosystems. Compliance with these regulations is essential for manufacturers aiming to market their products globally.
In conclusion, Carvacryl acetate, identified by CAS number 6380-28-5, is a multifaceted compound with significant potential across multiple industries. Its biological activities, synthetic versatility, and industrial applications make it a valuable asset in modern chemistry. As research progresses, we can expect even more innovative uses for this remarkable compound to emerge.
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