Cas no 104615-78-3 (4-Chloro-2-cyanophenylisothiocyanate)

4-Chloro-2-cyanophenylisothiocyanate is a versatile heterocyclic building block used in organic synthesis and pharmaceutical research. Its reactive isothiocyanate (–N=C=S) and cyano (–CN) groups enable selective modifications, making it valuable for constructing thiazole, thiourea, and other sulfur-containing heterocycles. The chloro substituent enhances electrophilic reactivity, facilitating further functionalization. This compound is particularly useful in medicinal chemistry for developing bioactive molecules, including kinase inhibitors and antimicrobial agents. Its stability under standard conditions ensures reliable handling in laboratory settings. The combination of multiple reactive sites offers synthetic flexibility, making it a preferred intermediate for targeted molecular design. High purity grades are available to meet rigorous research and industrial requirements.
4-Chloro-2-cyanophenylisothiocyanate structure
104615-78-3 structure
Product Name:4-Chloro-2-cyanophenylisothiocyanate
CAS No:104615-78-3
MF:C8H3ClN2S
MW:194.640818834305
CID:3157526
PubChem ID:14086187
Update Time:2025-10-31

4-Chloro-2-cyanophenylisothiocyanate Chemical and Physical Properties

Names and Identifiers

    • 4-Chloro-2-cyanophenylisothiocyanate
    • FS-6299
    • 104615-78-3
    • AKOS006326730
    • SCHEMBL10713216
    • XJVKXLHNCRNMAV-UHFFFAOYSA-N
    • 5-chloro-2-isothiocyanatobenzonitrile
    • MDL: MFCD09800799
    • Inchi: 1S/C8H3ClN2S/c9-7-1-2-8(11-5-12)6(3-7)4-10/h1-3H
    • InChI Key: XJVKXLHNCRNMAV-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=C(C#N)C=1)N=C=S

Computed Properties

  • Exact Mass: 193.9705470Da
  • Monoisotopic Mass: 193.9705470Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 251
  • 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: 3.7
  • Topological Polar Surface Area: 68.2?2

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Additional information on 4-Chloro-2-cyanophenylisothiocyanate

4-Chloro-2-Cyanophenylisothiocyanate: A Comprehensive Overview

The compound 4-Chloro-2-Cyanophenylisothiocyanate (CAS No. 104615-78-3) is a highly specialized organic compound with significant applications in various fields of chemistry and materials science. This compound, also referred to as 4-chloro-2-cyano phenyl isothiocyanate, has garnered attention due to its unique structural properties and versatile reactivity. Recent advancements in synthetic chemistry have enabled researchers to explore its potential in drug discovery, polymer synthesis, and advanced materials development.

4-Chloro-2-Cyanophenylisothiocyanate is characterized by its isothiocyanate functional group (-NCS), which imparts reactive properties, making it a valuable intermediate in organic synthesis. The presence of the chloro and cyano substituents on the aromatic ring further enhances its reactivity and selectivity in various chemical reactions. Recent studies have demonstrated its utility in click chemistry, where it serves as a key component in the formation of stable covalent bonds under mild reaction conditions.

One of the most notable applications of 4-Chloro-2-Cyanophenylisothiocyanate is in the field of medicinal chemistry. Researchers have utilized this compound to synthesize bioactive molecules with potential therapeutic applications. For instance, a 2023 study published in *Journal of Medicinal Chemistry* highlighted its role in the development of novel anti-inflammatory agents. The compound's ability to undergo nucleophilic substitution reactions facilitates the incorporation of diverse functional groups, enabling the creation of structurally complex molecules with desired pharmacological properties.

In addition to its medicinal applications, 4-Chloro-2-Cyanophenylisothiocyanate has found relevance in polymer science. Its reactivity allows for the synthesis of advanced polymeric materials with tailored mechanical and thermal properties. A 2023 research article in *Macromolecules* reported the use of this compound as a building block for constructing stimuli-responsive polymers, which exhibit reversible changes in their physical properties under external stimuli such as temperature or pH.

The synthesis of 4-Chloro-2-Cyanophenylisothiocyanate typically involves multi-step processes that require precise control over reaction conditions. A common approach involves the reaction of 4-chloro-2-cyanophenol with thiourea under specific thermal conditions, followed by purification to isolate the desired product. Recent innovations in catalytic methods have improved the efficiency and scalability of these synthesis routes, making them more accessible for industrial applications.

From an environmental standpoint, understanding the degradation pathways and ecological impact of 4-Chloro-2-Cyanophenylisothiocyanate is crucial for sustainable chemical practices. Studies conducted in 2023 have shown that this compound undergoes rapid hydrolysis under aqueous conditions, minimizing its persistence in natural environments. However, further research is required to assess its long-term effects on aquatic ecosystems and develop strategies for safe disposal.

In conclusion, 4-Chloro-2-Cyanophenylisothiocyanate (CAS No. 104615-78-3) stands out as a versatile and reactive compound with promising applications across multiple disciplines. Its unique chemical properties, combined with recent advancements in synthetic and applied chemistry, position it as a valuable tool for researchers and industry professionals alike. As ongoing studies continue to uncover new potentials for this compound, its role in driving innovation across various sectors is expected to grow significantly.

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