Cas no 114132-26-2 (Cyclopropylmethanesulfonyl chloride)

Cyclopropylmethanesulfonyl chloride is a versatile sulfonylating reagent used in organic synthesis, particularly for introducing the cyclopropylmethylsulfonyl group into target molecules. Its key advantages include high reactivity with nucleophiles, enabling efficient sulfonamide and sulfonate ester formation. The cyclopropyl ring confers steric and electronic effects that can influence the reactivity and stability of derived intermediates. This compound is valuable in pharmaceutical and agrochemical research for constructing sulfonamide-based scaffolds. It is typically handled under anhydrous conditions due to moisture sensitivity. The reagent's well-defined reactivity profile makes it a reliable choice for selective functionalization in complex synthetic routes.
Cyclopropylmethanesulfonyl chloride structure
114132-26-2 structure
Product Name:Cyclopropylmethanesulfonyl chloride
CAS No:114132-26-2
MF:C4H7ClO2S
MW:154.615179300308
MDL:MFCD10697744
CID:838119
PubChem ID:14106996
Update Time:2025-06-15

Cyclopropylmethanesulfonyl chloride Chemical and Physical Properties

Names and Identifiers

    • Cyclopropylmethanesulfonyl chloride
    • Cyclopropanemethanesulfonyl chloride
    • Cyclopropanemethanesulfonyl-chloride
    • AB60383
    • AGN-PC-000FCS
    • AK112915
    • cyclopropyl-methanesulfonyl chloride
    • Cyclopropylmethane-sulphonyl chloride
    • cyclopropylmethylsulfonyl chloride
    • EN300-76109
    • KB-251301
    • Cyclopropylmethanesulphonyl chloride
    • [(Chlorosulphonyl)methyl]cyclopropane
    • F1967-1619
    • 114132-26-2
    • cyclopropyl methanesulfonyl chloride
    • AKOS010297117
    • Cyclopropylmethanesulfonylchloride
    • Cyclopropylmethanesulfonyl chloride, AldrichCPR
    • XJPMSKSCGIBWPC-UHFFFAOYSA-N
    • 1-cyclopropylmethylsulfonyl chloride
    • SCHEMBL623476
    • DA-19770
    • CS-0054276
    • AS-42385
    • MFCD10697744
    • DTXSID10555955
    • SY045314
    • MDL: MFCD10697744
    • Inchi: 1S/C4H7ClO2S/c5-8(6,7)3-4-1-2-4/h4H,1-3H2
    • InChI Key: XJPMSKSCGIBWPC-UHFFFAOYSA-N
    • SMILES: ClS(CC1CC1)(=O)=O

Computed Properties

  • Exact Mass: 153.9855283g/mol
  • Monoisotopic Mass: 153.9855283g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 2
  • Complexity: 163
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.1
  • Topological Polar Surface Area: 42.5?2

Experimental Properties

  • Boiling Point: 224.143 ℃ at 760 mmHg

Cyclopropylmethanesulfonyl chloride Pricemore >>

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Additional information on Cyclopropylmethanesulfonyl chloride

Comprehensive Guide to Cyclopropylmethanesulfonyl chloride (CAS No. 114132-26-2): Properties, Applications, and Industry Insights

Cyclopropylmethanesulfonyl chloride (CAS No. 114132-26-2) is a specialized sulfonyl chloride derivative widely recognized for its role in organic synthesis and pharmaceutical intermediates. This compound, characterized by its cyclopropylmethane backbone and sulfonyl chloride functional group, has garnered significant attention in research and industrial applications due to its unique reactivity and versatility. In this article, we delve into its molecular properties, synthetic utility, and emerging trends aligned with current scientific and industrial demands.

The molecular structure of Cyclopropylmethanesulfonyl chloride features a cyclopropyl ring attached to a methanesulfonyl chloride moiety, which imparts high electrophilicity. This makes it a valuable reagent for nucleophilic substitution reactions, particularly in the synthesis of sulfonamides and sulfonate esters. Researchers frequently employ it as a sulfonylation agent to introduce the sulfonyl group into target molecules, a critical step in drug discovery and material science.

Recent advancements in green chemistry have spurred interest in optimizing the synthesis of Cyclopropylmethanesulfonyl chloride to minimize environmental impact. Innovations such as catalytic methods and solvent-free reactions are being explored to enhance efficiency and sustainability. These developments align with the growing demand for eco-friendly synthetic protocols, a topic frequently searched in academic and industrial forums.

In the pharmaceutical sector, Cyclopropylmethanesulfonyl chloride serves as a key intermediate for active pharmaceutical ingredients (APIs). Its application in constructing biologically active molecules is underscored by its role in modulating drug solubility and bioavailability. For instance, sulfonamide-based drugs derived from this compound are investigated for their potential in treating infectious diseases and metabolic disorders, addressing global health challenges.

Beyond pharmaceuticals, Cyclopropylmethanesulfonyl chloride finds utility in agrochemicals and specialty chemicals. Its incorporation into crop protection agents highlights its importance in sustainable agriculture, a sector increasingly focused on precision farming and reduced environmental footprint. This aligns with trending searches on agrochemical innovation and sustainable pest control.

Analytical techniques such as NMR spectroscopy, HPLC, and mass spectrometry are essential for characterizing Cyclopropylmethanesulfonyl chloride and ensuring its purity. Quality control remains a priority, especially for industries requiring high-purity reagents. Discussions on analytical method validation and impurity profiling are prevalent in scientific literature, reflecting user interest in reliable compound characterization.

Storage and handling of Cyclopropylmethanesulfonyl chloride require adherence to standard safety protocols, including moisture-free environments and inert atmospheres. While not classified as a hazardous material under this discussion, proper chemical storage practices are emphasized to maintain stability and prevent degradation, a topic frequently queried by laboratory professionals.

The future of Cyclopropylmethanesulfonyl chloride lies in its adaptability to cutting-edge research. With the rise of AI-driven drug discovery and automated synthesis platforms, this compound’s role in high-throughput screening and combinatorial chemistry is expanding. Such trends resonate with searches on digital transformation in chemistry and next-gen lab technologies.

In summary, Cyclopropylmethanesulfonyl chloride (CAS No. 114132-26-2) is a multifaceted compound with broad applications in pharmaceuticals, agrochemicals, and material science. Its synthesis, reactivity, and industrial relevance continue to evolve, driven by advancements in sustainable chemistry and technological integration. This guide aims to provide a holistic perspective while addressing contemporary queries and innovations in the field.

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