Cas no 1565675-37-7 (2-cyclopropylpropane-1-sulfonyl chloride)
2-cyclopropylpropane-1-sulfonyl chloride Chemical and Physical Properties
Names and Identifiers
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- 2-cyclopropylpropane-1-sulfonyl chloride
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- Inchi: 1S/C6H11ClO2S/c1-5(6-2-3-6)4-10(7,8)9/h5-6H,2-4H2,1H3
- InChI Key: LJPLUAIAXSGUSU-UHFFFAOYSA-N
- SMILES: C(S(Cl)(=O)=O)C(C1CC1)C
2-cyclopropylpropane-1-sulfonyl chloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-283688-0.05g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 0.05g |
$216.0 | 2025-03-19 | |
| Enamine | EN300-283688-0.1g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 0.1g |
$322.0 | 2025-03-19 | |
| Enamine | EN300-283688-0.25g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 0.25g |
$459.0 | 2025-03-19 | |
| Enamine | EN300-283688-0.5g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 0.5g |
$723.0 | 2025-03-19 | |
| Enamine | EN300-283688-1.0g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 1.0g |
$928.0 | 2025-03-19 | |
| Enamine | EN300-283688-2.5g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 2.5g |
$1819.0 | 2025-03-19 | |
| Enamine | EN300-283688-5.0g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 5.0g |
$2692.0 | 2025-03-19 | |
| Enamine | EN300-283688-10.0g |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95.0% | 10.0g |
$3992.0 | 2025-03-19 | |
| Ambeed | A1087048-1g |
2-Cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95% | 1g |
$755.0 | 2024-04-23 | |
| 1PlusChem | 1P01B3Z4-50mg |
2-cyclopropylpropane-1-sulfonyl chloride |
1565675-37-7 | 95% | 50mg |
$275.00 | 2025-03-19 |
2-cyclopropylpropane-1-sulfonyl chloride Related Literature
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
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Sowmyalakshmi Venkataraman RSC Adv., 2015,5, 73807-73813
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Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
Additional information on 2-cyclopropylpropane-1-sulfonyl chloride
2-Cyclopropylpropane-1-Sulfonyl Chloride: A Comprehensive Overview
2-Cyclopropylpropane-1-sulfonyl chloride, identified by the CAS number 1565675-37-7, is a chemical compound that has garnered significant attention in the fields of organic synthesis and materials science. This compound is a sulfonyl chloride derivative, characterized by its unique structure that combines a cyclopropyl group with a sulfonyl chloride moiety. The integration of these functional groups makes it a versatile building block in various chemical reactions, particularly in the synthesis of advanced materials and pharmaceutical intermediates.
The molecular structure of 2-cyclopropylpropane-1-sulfonyl chloride consists of a propane backbone, where the central carbon is attached to a cyclopropyl group and a sulfonyl chloride group. This configuration imparts distinctive electronic and steric properties to the molecule, enabling it to participate in a wide range of chemical transformations. Recent studies have highlighted its potential as a precursor for the synthesis of biodegradable polymers, which are increasingly sought after in sustainable materials development.
In terms of physical properties, 2-cyclopropylpropane-1-sulfonyl chloride exhibits a high boiling point due to the strong intermolecular forces arising from the sulfonyl chloride group. Its solubility in common organic solvents such as dichloromethane and THF makes it amenable to various synthetic protocols. Researchers have also explored its reactivity under different conditions, revealing its propensity to undergo nucleophilic substitution reactions, which are fundamental in organic synthesis.
The synthesis of 2-cyclopropylpropane-1-sulfonyl chloride typically involves the sulfonation of cyclopropane derivatives followed by chlorination. Recent advancements in catalytic methods have optimized this process, reducing reaction times and enhancing yield. These improvements have made the compound more accessible for industrial applications, particularly in the pharmaceutical sector where it serves as an intermediate in drug discovery programs targeting various therapeutic areas.
Beyond its role as a synthetic intermediate, 2-cyclopropylpropane-1-sulfonyl chloride has been investigated for its potential in energy storage applications. Studies have demonstrated that derivatives of this compound can act as cathode materials in lithium-ion batteries, offering improved energy density and cycle stability. This emerging application underscores the importance of understanding the electronic properties of sulfonyl chloride derivatives and their potential contributions to next-generation energy technologies.
In conclusion, 2-cyclopropylpropane-1-sulfonyl chloride (CAS No. 1565675-37-7) is a multifaceted compound with diverse applications across chemistry and materials science. Its unique structure and reactivity make it an invaluable tool in modern synthetic chemistry, while ongoing research continues to uncover new avenues for its utilization. As advancements in chemical synthesis and materials development proceed, this compound is poised to play an even greater role in shaping innovative solutions across various industries.
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