(+)-2-Chlorobutane (CAS 22156-91-8)
(+)-2-Chlorobutane (CAS:
22156-91-8) has molecular formula C4H9Cl and molecular weight 92.57 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 (+)-2-Chlorobutane.
Key Research Findings
- In addition, the secondary organic compounds formed due to the reactions were analysed qualitatively using GC-MS and then compared with the theoretical results of the individual
- EtP5 reveals stronger binding with 1-pentene the accompanying change of energy upon the complexation being 85.5 kJ mol compared to 71.3 and 75.8 kJ mol for the cis and trans-2-pe
- Several classic molecular sorbents show high selectivity in the context of such separations; however, most suffer from limited tunability or poor stability.
- The adsorption of trace CB isomers results in the formation of new CB-loaded crystal structures, whose thermostability is higher than their corresponding isomer-loaded structures
Detailed Literature Analysis
Below are the top-ranked research papers for (+)-2-Chlorobutane, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Atmospheric reactions of substituted butanes with OH radicals: kinetics and atmospheric implications.
2-Chlorobutane (2CB) and 2-aminobutane (2AB) are chiral compounds, which play a crucial role in biological complexity. These compounds can be released into the air through natural and man-made processes. Their emission into the atmosphere may influence the air quality and climate significantly. In the present work, the kinetics for the reaction
Other Research
2. Probing Binding of Ethylated Pillar[5]arene with Pentene and Chlorobutane Positional Isomers.
Host guest binding from alkyl-modified pillararene macrocycles has been of significant interest in a variety of applications in the domains of supramolecular chemistry. In this work, we analyze the selectivity in binding of the ethylated pillar[5]arene (EtP5) macrocycle with 1-pentene, cis and trans 2-pentene, and the 1- and 2-chlorobutane isom
3. Tuning the porosity of triangular supramolecular adsorbents for superior haloalkane isomer separations.
Distillation-free separations of haloalkane isomers represents a persistent challenge for the chemical industry. Several classic molecular sorbents show high selectivity in the context of such separations; however, most suffer from limited tunability or poor stability. Herein, we report the results of a comparative study involving three triangl
4. Highly Selective Removal of Trace Isomers by Nonporous Adaptive Pillararene Crystals for Chlorobutane Purification.
Removal of trace chlorobutane (CB) isomers is highly desired to produce high grade 1-chlorobutane (1-CB) and 2-chlorobutane (2-CB). Here, we report that nonporous adaptive crystals (NACs) of perethylated pillar[5]arene (EtP5) and pillar[6]arene (EtP6) effectively remove trace CB isomers. EtP5 NACs can remove trace 1-CB (2%) from 2-CB to improve
Conclusion
The research literature on (+)-2-Chlorobutane 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.