((Isopentyloxy)methyl)oxirane (CAS 15965-97-6)
((Isopentyloxy)methyl)oxirane (CAS:
15965-97-6) has molecular formula C8H16O2 and molecular weight 144.21 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 ((Isopentyloxy)methyl)oxirane.
Key Research Findings
- However, the exhaustive exploration of a reactive network is often a daunting task, resulting in unexplored reactive channels that affect kinetic outcomes and branching ratios.
- The -CHDO to -CHO ratio is found to be 0.15 corresponding to a D-to-H ratio of 0.036 per H atom which is slightly higher than the D-to-H ratio of species such as methanol, formalde
Detailed Literature Analysis
Below are the top-ranked research papers for ((Isopentyloxy)methyl)oxirane, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Automated Exploration of Radical-Molecule Chemistry: The Case of Oxirane + CH in the ISM
Quantum chemistry provides accurate and reliable methods to investigate reaction pathways of reactive molecular systems relevant to the interstellar medium. However, the exhaustive exploration of a reactive network is often a daunting task, resulting in unexplored reactive channels that affect kinetic outcomes and branching ratios. Here, an automat
🔑 Key Finding: However, the exhaustive exploration of a reactive network is often a daunting task, resulting in unexplored reactive channels that affect kinetic outcomes and branching ratios.
2. Automated Exploration of Radical-Molecule Chemistry: The Case of Oxirane + CH in the ISM
Quantum chemistry provides accurate and reliable methods to investigate reaction pathways of reactive molecular systems relevant to the interstellar medium. However, the exhaustive exploration of a reactive network is often a daunting task, resulting in unexplored reactive channels that affect kinetic outcomes and branching ratios. Here, an automat
3. Rotational spectroscopy of mono-deuterated oxirane (-CHDO) and its detection towards IRAS 162932422 B
We prepared a sample of mono-deuterated oxirane and studied its rotational spectrum in the laboratory between 490 GHz and 1060 GHz in order to improve its spectroscopic parameters and consequently the calculated rest frequencies of its rotational transitions. The updated rest frequencies were employed to detect -CHDO for the first time in the inter
4. Rotational spectroscopy of mono-deuterated oxirane (-CHDO) and its detection towards IRAS 162932422 B
We prepared a sample of mono-deuterated oxirane and studied its rotational spectrum in the laboratory between 490 GHz and 1060 GHz in order to improve its spectroscopic parameters and consequently the calculated rest frequencies of its rotational transitions. The updated rest frequencies were employed to detect -CHDO for the first time in the inter
5. Tracing potential energy surfaces of electronic excitations via their transition origins: application to Oxirane
We show that the transition origins of electronic excitations identified by quantified natural transition orbital (QNTO) analysis can be employed to connect potential energy surfaces (PESs) according to their character across a widerange of molecular geometries. This is achieved by locating the switching of transition origins of adiabatic potential
6. Troubleshooting Time-Dependent Density-Functional Theory for Photochemical Applications: Oxirane
The development of analytic-gradient methodology for excited states within conventional time-dependent density-functional theory (TDDFT) would seem to offer a relatively inexpensive alternative to better established quantum-chemical approaches for the modeling of photochemical reactions. However, even though TDDFT is formally exact, practical calcu
7. Tracing potential energy surfaces of electronic excitations via their transition origins: application to Oxirane
We show that the transition origins of electronic excitations identified by quantified natural transition orbital (QNTO) analysis can be employed to connect potential energy surfaces (PESs) according to their character across a widerange of molecular geometries. This is achieved by locating the switching of transition origins of adiabatic potential
8. Troubleshooting Time-Dependent Density-Functional Theory for Photochemical Applications: Oxirane
The development of analytic-gradient methodology for excited states within conventional time-dependent density-functional theory (TDDFT) would seem to offer a relatively inexpensive alternative to better established quantum-chemical approaches for the modeling of photochemical reactions. However, even though TDDFT is formally exact, practical calcu
Conclusion
The research literature on ((Isopentyloxy)methyl)oxirane 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. 8 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.