Cas no 165528-81-4 (tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate)
tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate Chemical and Physical Properties
Names and Identifiers
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- 4-(2-Boc-aminoethyl)piperidine
- (2-PIPERIDIN-4-YL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER
- tert-Butyl (2-(piperidin-4-yl)ethyl)carbamate
- 4-(2-Aminoethyl)piperidine, 4-BOC protected
- tert-butyl N-(2-piperidin-4-ylethyl)carbamate
- 4-(BOC-AMINOETHYL)PIPERIDINE
- 4-(N-BOC-2-AMINOETHYL)PIPERIDINE
- 4-(2-BOC-AMINOETHYL)-1-PIPERIDINE
- 4-(2-Aminothyl)piperidine,N2-BOC protected
- TERT-BUTYL (2-PIPERIDIN-4-YLETHYL)CARBAMATE
- 4-(2-Aminoethyl)piperidine, N2-BOC protected
- Carbamic acid, N-[2-(4-piperidinyl)ethyl]-, 1,1-dimethylethyl ester
- tert-butyl 2-(piperidin-4-yl)ethylcarbamate
- 4-(2-Boc-aminoethyl) piperidine
- 4-[2-(Boc-amino)ethyl]piperidine
- tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate
- Carbamic acid, [2-(4-piperidinyl)ethyl]-, 1,1-dimethylethyl ester
- Carbamic acid, N-[2-(4-piperi
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- MDL: MFCD01318373
- Inchi: 1S/C12H24N2O2/c1-12(2,3)16-11(15)14-9-6-10-4-7-13-8-5-10/h10,13H,4-9H2,1-3H3,(H,14,15)
- InChI Key: RQRMFFGCUUGYPC-UHFFFAOYSA-N
- SMILES: O(C(NCCC1CCNCC1)=O)C(C)(C)C
Computed Properties
- Exact Mass: 228.18400
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 16
- Rotatable Bond Count: 5
- Complexity: 218
- Topological Polar Surface Area: 50.4
Experimental Properties
- Boiling Point: 337.3℃ at 760 mmHg
- PSA: 50.36000
- LogP: 2.62050
tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate Customs Data
- HS CODE:2933399090
- Customs Data:
China Customs Code:
2933399090Overview:
2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | P822030-1g |
(2-PIPERIDIN-4-YL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER |
165528-81-4 | 98% | 1g |
843.00 | 2021-05-17 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | P49340-5g |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 5g |
¥1716.0 | 2021-09-08 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | P49340-1g |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 1g |
¥436.0 | 2021-09-08 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | P49340-250mg |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 250mg |
¥256.0 | 2021-09-08 | ||
| TRC | B603355-100mg |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 100mg |
$ 64.00 | 2023-04-18 | ||
| TRC | B603355-250mg |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 250mg |
$ 87.00 | 2023-04-18 | ||
| TRC | B603355-500mg |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 500mg |
$ 138.00 | 2023-04-18 | ||
| TRC | B603355-1g |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 1g |
$ 150.00 | 2022-06-07 | ||
| Alichem | A129003961-5g |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 95% | 5g |
$288.32 | 2022-04-02 | |
| Alichem | A129003961-10g |
4-(2-Boc-aminoethyl)piperidine |
165528-81-4 | 95% | 10g |
$480.20 | 2022-04-02 |
tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate Related Literature
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Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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3. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
Additional information on tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate
Introduction to tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate (CAS No. 165528-81-4)
Tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate, identified by its Chemical Abstracts Service (CAS) number 165528-81-4, is a specialized organic compound that has garnered significant attention in the field of pharmaceutical chemistry and medicinal research. This compound belongs to the class of carbamates, which are known for their versatile applications in drug development due to their stability and reactivity. The structural features of tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate, particularly the presence of a tert-butyl group and a piperidine moiety, contribute to its unique chemical properties and potential biological activities.
The tert-butyl group is a branched alkyl group that enhances the lipophilicity of the molecule, making it more suitable for membrane permeability and improving pharmacokinetic profiles. This characteristic is particularly valuable in drug design, where optimizing bioavailability is a critical consideration. On the other hand, the piperidine ring is a common pharmacophore found in many bioactive molecules, including antipsychotics, antivirals, and cardiovascular drugs. Its presence in tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate suggests potential interactions with biological targets, which may be exploited for therapeutic purposes.
In recent years, there has been a growing interest in carbamate derivatives as they exhibit a wide range of biological activities. Research has shown that carbamates can serve as intermediates in the synthesis of various pharmacologically active compounds. The specific structure of tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate positions it as a promising candidate for further investigation in medicinal chemistry. Its ability to undergo various chemical transformations makes it a valuable building block for the development of novel drugs.
One of the most compelling aspects of tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate is its potential role in modulating enzyme activity. Enzymes are central to many biological processes, and their inhibition or activation can lead to therapeutic effects. The combination of the tert-butyl group and the piperidine moiety may allow this compound to interact with specific enzyme sites, thereby influencing metabolic pathways or signal transduction processes. This possibility has opened up avenues for research into its potential applications in treating various diseases.
Recent studies have also explored the use of carbamates in addressing neurological disorders. The piperidine ring, in particular, has been associated with compounds that show promise in treating conditions such as Parkinson's disease and epilepsy. By investigating tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate, researchers aim to uncover new mechanisms of action that could lead to more effective treatments for these conditions. The compound's structural features make it an attractive candidate for further exploration in this field.
The synthesis of tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate involves multi-step organic reactions that require precise control over reaction conditions. The introduction of the tert-butyl group and the piperidine moiety necessitates careful selection of reagents and catalysts to ensure high yield and purity. Advances in synthetic methodologies have made it possible to produce this compound with increasing efficiency, which is crucial for large-scale pharmaceutical applications.
In addition to its potential therapeutic applications, tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate may also find utility in chemical research as a model compound for studying carbamate reactivity and stability. Understanding how this compound behaves under different conditions can provide insights into broader chemical principles, which can be applied to other molecules with similar structures.
The growing body of research on carbamates underscores their importance in modern drug discovery. As scientists continue to explore new synthetic routes and biological activities, compounds like tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate are likely to play a significant role in developing next-generation therapeutics. Their unique structural features offer a rich foundation for innovation, making them indispensable tools in pharmaceutical chemistry.
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