Cas no 70275-54-6 (Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate)
Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate Chemical and Physical Properties
Names and Identifiers
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- Carbamic acid, [2-(4-hydroxyphenyl)ethyl]-, ethyl ester(9CI)
- [2-(4-HYDROXY-PHENYL)-ETHYL]-CARBAMIC ACID ETHYL ESTER
- 2-(4-Hydroxyphenyl)ethylcarbamic acid ethyl ester
- Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate
- ethylhydroxyphenylethylcarbamate
- N-Carbaethoxy-tyramin
- N-Ethoxycarbonyl-tyramin
- SCHEMBL580001
- Ethyl 4-hydroxyphenethylcarbamate
- CHEMBL5003984
- AKOS005765965
- [2-(4-HYDROXY-PHENYL)-ETHYL]-CARBAMICACIDETHYLESTER
- ethyl (4-hydroxyphenethyl)carbamate
- MFCD02682912
- FT-0608648
- DTXSID80376194
- J-521031
- Carbamic acid,[2-(4-hydroxyphenyl)ethyl]-,ethyl ester(9ci)
- SS-4038
- [2-(4-hydroxy-phenyl)-ethyl]carbamic acid ethyl ester
- PTGMINZYLYOVNN-UHFFFAOYSA-N
- 70275-54-6
- Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate
-
- MDL： MFCD02682912
- Inchi： 1S/C11H15NO3/c1-2-15-11(14)12-8-7-9-3-5-10(13)6-4-9/h3-6,13H,2,7-8H2,1H3,(H,12,14)
- InChI Key： PTGMINZYLYOVNN-UHFFFAOYSA-N
- SMILES： O(CC)C(NCCC1C=CC(=CC=1)O)=O
Computed Properties
- Exact Mass: 209.10500
- Monoisotopic Mass: 209.10519334g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 15
- Rotatable Bond Count: 6
- Complexity: 188
- 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
- XLogP3: 1.9
- Topological Polar Surface Area: 58.6?2
Experimental Properties
- Density: 1.146
- Boiling Point: 387 oC
- Flash Point: 188 oC
- PSA: 58.56000
- LogP: 2.07170
Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate Customs Data
- HS CODE：2924299090
- Customs Data：
China Customs Code:
2924299090Overview:
2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, packing
Summary:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019146788-1g |
Ethyl 4-hydroxyphenethylcarbamate |
70275-54-6 | 95% | 1g |
$400.00 | 2023-09-01 | |
| abcr | AB303772-500 mg |
Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate; 95% |
70275-54-6 | 500MG |
€267.70 | 2022-03-25 | ||
| abcr | AB303772-1 g |
Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate; 95% |
70275-54-6 | 1g |
€349.50 | 2022-03-25 | ||
| Chemenu | CM133311-1g |
ethyl (4-hydroxyphenethyl)carbamate |
70275-54-6 | 95% | 1g |
$298 | 2024-07-24 | |
| TRC | E047925-50mg |
Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate |
70275-54-6 | 50mg |
$ 145.00 | 2022-06-05 | ||
| TRC | E047925-100mg |
Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate |
70275-54-6 | 100mg |
$ 240.00 | 2022-06-05 | ||
| abcr | AB303772-500mg |
Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate, 95%; . |
70275-54-6 | 95% | 500mg |
€315.00 | 2024-06-08 | |
| abcr | AB303772-1g |
Ethyl N-[2-(4-hydroxyphenyl)ethyl]carbamate, 95%; . |
70275-54-6 | 95% | 1g |
€478.80 | 2024-06-08 | |
| A2B Chem LLC | AC74861-1mg |
Ethyl 4-hydroxyphenethylcarbamate |
70275-54-6 | >95% | 1mg |
$201.00 | 2024-04-19 | |
| A2B Chem LLC | AC74861-5mg |
Ethyl 4-hydroxyphenethylcarbamate |
70275-54-6 | >95% | 5mg |
$214.00 | 2024-04-19 |
Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate Related Literature
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
Additional information on Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate
Ethyl N-2-(4-Hydroxyphenyl)Ethylcarbamate: A Comprehensive Overview
Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate, with the CAS number 70275-54-6, is a compound of significant interest in various scientific and industrial applications. This compound, often referred to as Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate, belongs to the class of carbamates and is characterized by its unique chemical structure. The compound's structure includes a hydroxyl group attached to a phenyl ring, which plays a crucial role in its reactivity and functionality. Recent studies have highlighted its potential in fields such as pharmacology, material science, and environmental chemistry.
The CAS number 70275-54-6 serves as a unique identifier for this compound, ensuring consistency in scientific communication and regulatory compliance. The compound's chemical formula is C11H13NO3, with a molecular weight of 199.23 g/mol. Its physical properties include a melting point of approximately 85°C and a boiling point around 300°C. These properties make it suitable for various synthetic processes and applications.
Recent advancements in synthetic chemistry have led to innovative methods for the production of Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate. One notable approach involves the reaction of 4-hydroxyaniline with ethyl chloroformate under controlled conditions. This method not only enhances the yield but also ensures the purity of the final product. Researchers have also explored the use of catalytic systems to optimize the reaction kinetics, making the synthesis more efficient and environmentally friendly.
In terms of applications, Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate has shown promise in the pharmaceutical industry as a precursor for bioactive compounds. Its ability to form stable amide bonds makes it an ideal candidate for drug delivery systems and therapeutic agents. For instance, studies have demonstrated its potential as an intermediate in the synthesis of antiviral and anticancer drugs.
Moreover, this compound has gained attention in material science due to its ability to form cross-linked polymers with desirable mechanical properties. The hydroxyl group present in its structure facilitates polymerization reactions, leading to materials with enhanced durability and flexibility. These materials have potential applications in coatings, adhesives, and composite manufacturing.
Environmental considerations are another area where Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate has proven valuable. Recent research has focused on its role in biodegradable plastics and eco-friendly packaging solutions. The compound's ability to undergo enzymatic degradation makes it a sustainable alternative to traditional petroleum-based plastics.
In conclusion, Ethyl N-2-(4-hydroxyphenyl)ethylcarbamate (CAS number 70275-54-6) is a versatile compound with a wide range of applications across multiple disciplines. Its unique chemical properties, combined with recent advancements in synthesis and application techniques, position it as a key player in modern scientific research and industrial innovation.
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