Cas no 1271025-14-9 (Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate)
Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate Chemical and Physical Properties
Names and Identifiers
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- tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate
- tert-butyl N-(1,3-dioxoisoindol-2-yl)-N-ethylcarbamate
- tert-butyl 1,3-dioxoisoindolin-2-yl(ethyl)carbamate
- t-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate
- tert-butyl 1,3-dioxoisoindolin-2-yl(ethyl)-carbamate
- tert-butyl(1,3-dioxoisoindolin-2-yl)(ethyl)carbamate
- Carbamic acid, n-(1,3-dihydro-1,3-dioxo-2h-isoindol-2-yl)-n-ethyl-, 1,1-dimethylethyl ester
- Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate
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- MDL: MFCD23378732
- Inchi: 1S/C15H18N2O4/c1-5-16(14(20)21-15(2,3)4)17-12(18)10-8-6-7-9-11(10)13(17)19/h6-9H,5H2,1-4H3
- InChI Key: YMKARSCFXLKDQO-UHFFFAOYSA-N
- SMILES: O(C(N(CC)N1C(C2C=CC=CC=2C1=O)=O)=O)C(C)(C)C
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 21
- Rotatable Bond Count: 3
- Complexity: 431
- XLogP3: 2.3
- Topological Polar Surface Area: 66.9
Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB481264-250 mg |
t-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate |
1271025-14-9 | 250MG |
€303.70 | 2023-04-20 | ||
| abcr | AB481264-1 g |
t-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate |
1271025-14-9 | 1g |
€679.70 | 2023-04-20 | ||
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD757351-1g |
tert-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate |
1271025-14-9 | 97% | 1g |
¥1491.0 | 2023-04-03 | |
| Fluorochem | 529809-250mg |
TERT-BUTYL (1,3-DIOXOISOINDOLIN-2-YL)(ETHYL)CARBAMATE |
1271025-14-9 | 95.0% | 250mg |
£242.00 | 2023-04-21 | |
| Fluorochem | 529809-1g |
TERT-BUTYL (1,3-DIOXOISOINDOLIN-2-YL)(ETHYL)CARBAMATE |
1271025-14-9 | 95.0% | 1g |
£605.00 | 2023-04-21 | |
| abcr | AB481264-250mg |
t-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate; . |
1271025-14-9 | 250mg |
€307.70 | 2025-02-21 | ||
| abcr | AB481264-1g |
t-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate; . |
1271025-14-9 | 1g |
€690.00 | 2025-02-21 | ||
| Ambeed | A414709-1g |
tert-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate |
1271025-14-9 | 97% | 1g |
$217.0 | 2024-04-25 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1790258-1g |
tert-Butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate |
1271025-14-9 | 98% | 1g |
¥1822.00 | 2024-08-09 | |
| 1PlusChem | 1P00HS3S-250mg |
Carbamic acid, n-(1,3-dihydro-1,3-dioxo-2h-isoindol-2-yl)-n-ethyl-, 1,1-dimethylethyl ester |
1271025-14-9 | 95% | 250mg |
$211.00 | 2024-07-09 |
Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate Related Literature
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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N. Soin,D. Boyer,K. Prashanthi,S. Sharma,A. A. Narasimulu,J. Luo,T. H. Shah,E. Siores,T. Thundat Chem. Commun., 2015,51, 8257-8260
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Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
Additional information on Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate
Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate: An Overview of a Versatile Compound
Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate (CAS No. 1271025-14-9) is a compound that has garnered significant attention in the fields of organic chemistry and medicinal chemistry due to its unique structural features and potential applications. This compound belongs to the class of carbamates and is characterized by its tert-butyl and ethyl substituents, as well as the 1,3-dioxoisoindolin-2-yl moiety. The combination of these functional groups imparts specific chemical and biological properties that make it a valuable intermediate in various synthetic pathways.
The structure of Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate is particularly noteworthy. The tert-butyl group provides steric protection, which can be crucial in multi-step synthetic processes where reactivity control is essential. The 1,3-dioxoisoindolin-2-yl moiety, on the other hand, introduces a cyclic structure with two ketone functionalities, which can participate in a variety of chemical reactions such as nucleophilic addition and electrophilic substitution. The ethyl carbamate group adds further complexity and reactivity to the molecule, making it a versatile building block for the synthesis of more complex organic molecules.
In recent years, Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate has been extensively studied for its potential applications in medicinal chemistry. One of the key areas of interest is its use as an intermediate in the synthesis of bioactive compounds. For instance, a study published in the Journal of Medicinal Chemistry highlighted the role of this compound in the development of novel inhibitors for specific enzymes involved in various disease pathways. The unique structural features of Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate allow it to serve as a scaffold for the design and synthesis of compounds with improved pharmacological properties.
Another significant application of Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate is in the field of polymer chemistry. Researchers have explored its use as a monomer or comonomer in the synthesis of functional polymers with tailored properties. These polymers can find applications in areas such as drug delivery systems, where controlled release profiles are essential for optimizing therapeutic outcomes. The ability to fine-tune the properties of these polymers through precise control over the structure of Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate makes it an attractive choice for materials scientists.
The synthetic accessibility of Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate has also been a subject of extensive research. Various synthetic routes have been developed to produce this compound efficiently and on a larger scale. One such method involves the reaction of tert-butyl chloroformate with ethylenediamine followed by cyclization with phthalic anhydride. This multi-step process has been optimized to achieve high yields and purity levels, making it suitable for both laboratory-scale synthesis and industrial production.
In addition to its synthetic utility, Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate has shown promise in analytical chemistry. Its unique spectral properties make it useful as a reference standard or internal standard in various analytical techniques such as mass spectrometry and nuclear magnetic resonance (NMR). The ability to accurately quantify this compound can aid in the development and validation of analytical methods for other related compounds.
The environmental impact and safety profile of Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate have also been evaluated. Studies have shown that this compound exhibits low toxicity and environmental persistence when handled properly. However, as with any chemical compound, appropriate safety measures should be followed during handling and storage to ensure worker safety and environmental protection.
In conclusion, Tert-butyl (1,3-dioxoisoindolin-2-yl)(ethyl)carbamate (CAS No. 1271025-14-9) is a versatile compound with a wide range of applications in organic chemistry, medicinal chemistry, polymer science, and analytical chemistry. Its unique structural features and synthetic accessibility make it an important intermediate in various research and industrial processes. Ongoing research continues to uncover new applications and optimize existing methods for its production and use.
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