Cas no 115766-13-7 ((S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate)
(S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate Chemical and Physical Properties
Names and Identifiers
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- Carbamic acid,[1-(cyclohexylmethyl)-2-(methoxymethylamino)-2-oxoethyl]-,1,1-dimethylethyl ester, (S)-
- (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate
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- Inchi: 1S/C16H30N2O4/c1-16(2,3)22-15(20)17-13(14(19)18(4)21-5)11-12-9-7-6-8-10-12/h12-13H,6-11H2,1-5H3,(H,17,20)/t13-/m0/s1
- InChI Key: SCJHTSDYKFTJSN-ZDUSSCGKSA-N
- SMILES: C(OC(C)(C)C)(=O)N[C@@H](CC1CCCCC1)C(N(OC)C)=O
(S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| AN HUI ZE SHENG Technology Co., Ltd. | PH001570-1mg |
115766-13-7 | 1mg |
¥2041.72 | 2023-09-15 |
(S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate Related Literature
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
Additional information on (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate
Research Brief on (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate (CAS: 115766-13-7)
The compound (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate (CAS: 115766-13-7) has garnered significant attention in recent chemical and pharmaceutical research due to its potential applications in drug discovery and development. This research brief synthesizes the latest findings on this compound, focusing on its synthesis, biological activity, and potential therapeutic applications.
Recent studies have highlighted the role of this compound as a key intermediate in the synthesis of peptide-based therapeutics. Its unique structural features, including the tert-butyl carbamate protecting group and the methoxy(methyl)amino moiety, make it a versatile building block for the construction of complex molecules. Researchers have successfully employed it in the synthesis of protease inhibitors and other bioactive peptides, demonstrating its utility in medicinal chemistry.
In terms of biological activity, preliminary investigations suggest that derivatives of (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate exhibit promising inhibitory effects against specific enzymatic targets. For instance, a 2023 study published in the Journal of Medicinal Chemistry reported its efficacy in modulating the activity of certain serine proteases, which are implicated in various pathological conditions, including inflammation and cancer.
The synthesis of this compound has also been optimized in recent years. A 2022 paper in Organic Process Research & Development detailed a scalable and cost-effective route for its production, emphasizing the use of environmentally benign reagents and conditions. This advancement is particularly significant for industrial applications, where scalability and sustainability are critical considerations.
Looking ahead, researchers are exploring the potential of (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate in the development of novel therapeutics. Its structural flexibility and demonstrated bioactivity make it a promising candidate for further investigation. Future studies are expected to focus on its mechanism of action, pharmacokinetics, and in vivo efficacy, which will be crucial for its transition from the laboratory to clinical applications.
In conclusion, (S)-tert-butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate represents a valuable tool in chemical biology and drug discovery. Its synthesis, biological activity, and potential therapeutic applications underscore its importance in contemporary research. Continued exploration of this compound is likely to yield significant insights and innovations in the field of medicinal chemistry.
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