(+)-1,5,5-trimethyl-2-thiabicyclo[2.2.2]octane (CAS 19296-90-3)
(+)-1,5,5-trimethyl-2-thiabicyclo[2.2.2]octane (CAS:
19296-90-3) has molecular formula C10H18S and molecular weight 170.32 g/mol. This compound has been the subject of numerous scientific investigations due to its structural features and practical utility in synthetic chemistry and industrial processes. View product details →
Product Background
This comprehensive research profile examines the scientific literature surrounding (+)-1,5,5-trimethyl-2-thiabicyclo[2.2.2]octane.
Key Research Findings
- Multimodal characterization and theoretical simulations reveal that Selectfluor favorably modifies the Li solvation structure by displacing solvent molecules and promoting anion
- All of the compounds exhibited significant inhibition against the diabetic target alpha-glucosidase, with low to submicromole IC values , and the binding modes of selected molecu
- Compound 17 showed significant alpha-glucosidase inhibitory activity with IC value of 19.96 +/- 0.32 muM.
- The microstructure of the puffed sea cucumber exhibited a uniform porous structure at 230 degrees C for 4 min.
Detailed Literature Analysis
Below are the top-ranked research papers for (+)-1,5,5-trimethyl-2-thiabicyclo[2.2.2]octane, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Engineering interfacial chemistry and solvation structure via a novel ionic additive for ⁓5 V-class LiNi(0.5)Mn(1.5)O(4) batteries.
Despite the high energy density and voltage plateau offered by approximately 5 V-class lithium-metal batteries using spinel LiNi(0.5)Mn(1.5)O(4) (LNMO) cathodes and lithium metal anodes, their practical application is hindered by rapid capacity degradation due to severe electrolyte decomposition, transition-metal dissolution, and lithium dendr
2. Structurally Diverse Stilbenoids as Potent α-Glucosidase Inhibitors with Antidiabetic Effect from Morus alba.
Fifteen stilbenoid derivatives, including five previously undescribed ones (albaphenols A-E, 1-5) with diverse scaffolds, were obtained from the well-known agricultural economic tree Morus alba. Their structures, including absolute stereochemistries, were fully characterized by detailed interpretation of spectroscopic data and quantum chemical
Biological & Pharmacological Studies
3. Anti-diabetic and anti-inflammatory indole diterpenes from the marine-derived fungus Penicillium sp. ZYX-Z-143.
Seven new indole-diterpenoids, penpaxilloids A-E (1-5), 7-methoxypaxilline-13-ene (6), and 10-hydroxy-paspaline (7), along with 20 known ones (8-27), were isolated from the marine-derived fungus Penicillium sp. ZYX-Z-143. Among them, compound 1 was a spiro indole-diterpenoid bearing a 2,3,3a,5-tetrahydro-1H-benzo[d]pyrrolo[2,1-b][1,3]oxazin-1-o
4. The dynamic changes of flavor characteristics of sea cucumber (Apostichopus japonicus) during puffing revealed by GC-MS combined with HS-GC-IMS.
To improve the ease of eating sea cucumbers, we investigated the impact of puffing temperature (190 degrees C - 250 degrees C) and time (1-5 min) on their quality and flavor. As temperature and time increased, sea cucumber puffing significantly enhanced. The microstructure of the puffed sea cucumber exhibited a uniform porous structure at 230
Conclusion
The research literature on (+)-1,5,5-trimethyl-2-thiabicyclo[2.2.2]octane demonstrates sustained scientific interest, with publications continuing through 0. The compound serves as an important building block in synthetic chemistry and has been explored for various applications. Researchers and industrial users can view detailed specifications or submit an inquiry for pricing and availability.
Data Sources: PubMed/MEDLINE, CrossRef. 4 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.