Cas no 52928-01-5 (4-iodobenzene-1-thiol)

4-Iodobenzene-1-thiol (CAS: 10015-09-9) is a sulfur-containing aromatic compound featuring an iodine substituent at the para position. This organosulfur reagent is valued for its utility in cross-coupling reactions, particularly in the synthesis of thiol-functionalized materials and metal-organic frameworks. The iodine moiety enhances reactivity in palladium-catalyzed transformations, such as Suzuki or Sonogashira couplings, while the thiol group enables surface modification and ligand anchoring in nanomaterials. Its stability under controlled conditions and compatibility with diverse synthetic protocols make it a versatile intermediate in organic and materials chemistry. Suitable for use under inert atmospheres, it is commonly handled in solution to minimize oxidation.
4-iodobenzene-1-thiol structure
4-iodobenzene-1-thiol structure
Product Name:4-iodobenzene-1-thiol
CAS No:52928-01-5
MF:C6H5IS
MW:236.073372602463
MDL:MFCD01632442
CID:358452
PubChem ID:656900
Update Time:2025-10-31

4-iodobenzene-1-thiol Chemical and Physical Properties

Names and Identifiers

    • 4-iodobenzene-1-thiol
    • 4-iodobenzenethiol
    • Benzenethiol, 4-iodo-
    • 4-IODO-BENZENETHIOL (WITH THE DIMMER IMPURITY)
    • 4-Iodo-benzenethiol (with the dimer impurity)
    • AS-83007
    • 52928-01-5
    • CCA92801
    • p-iodothiophenol
    • IKZUTVQEBGHQJA-UHFFFAOYSA-N
    • MFCD01632442
    • SCHEMBL48310
    • F20637
    • DTXSID40349667
    • 4-iodothiophenol
    • EN300-184001
    • DB-332364
    • MDL： MFCD01632442
    • Inchi： 1S/C6H5IS/c7-5-1-3-6(8)4-2-5/h1-4,8H
    • InChI Key： IKZUTVQEBGHQJA-UHFFFAOYSA-N
    • SMILES： IC1C=CC(=CC=1)S

Computed Properties

  • Exact Mass: 235.91525
  • Monoisotopic Mass: 235.91567g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 0
  • Complexity: 66.9
  • 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: 3.4
  • Topological Polar Surface Area: 1?2

Experimental Properties

  • PSA: 0

4-iodobenzene-1-thiol Pricemore >>

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4-iodobenzene-1-thiol Suppliers

Amadis Chemical Company Limited
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(CAS:52928-01-5)4-iodobenzene-1-thiol
Order Number:A1163874
Stock Status:in Stock
Quantity:250.0mg/1.0g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 00:19
Price ($):251.0/752.0

4-iodobenzene-1-thiol Related Literature

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Additional information on 4-iodobenzene-1-thiol

4-IodoBenzenethiol: A Comprehensive Overview

The compound with CAS No 52928-01-5, commonly referred to as 4-IodoBenzenethiol, is a significant molecule in the field of organic chemistry. This compound, also known as 4-iodobenzene thiol, has garnered attention due to its unique properties and versatile applications in various scientific domains. Recent advancements in chemical synthesis and material science have further highlighted its potential in cutting-edge research.

4-IodoBenzenethiol is an aromatic thiol derivative with a molecular formula of C7H5IOS. Its structure consists of a benzene ring substituted with an iodine atom at the para position and a thiol (-SH) group at the ortho position. This arrangement imparts the molecule with distinct electronic and steric properties, making it valuable for specific chemical reactions and material applications.

The synthesis of 4-IodoBenzenethiol typically involves multi-step processes, including nucleophilic substitution and coupling reactions. Recent studies have explored more efficient methodologies to enhance yield and purity, leveraging advanced catalysts and reaction conditions. For instance, researchers have employed transition metal catalysts to facilitate coupling reactions, significantly improving the overall process.

In terms of applications, 4-IodoBenzenethiol has found utility in the development of advanced materials, particularly in the field of electronics. Its ability to form self-assembled monolayers (SAMs) on various substrates has made it a key component in nanotechnology and surface science. SAMs formed by 4-IodoBenzenethiol exhibit excellent stability and functionality, making them ideal for use in sensors, catalysis, and drug delivery systems.

Recent research has also explored the use of 4-IodoBenzenethiol in biochemistry and pharmacology. The molecule's thiol group enables it to participate in redox reactions, which are critical in biological systems. Studies have demonstrated its potential as a precursor for synthesizing bioactive compounds, including antioxidants and anti-inflammatory agents.

The electronic properties of 4-IodoBenzenethiol make it a promising candidate for optoelectronic devices. Its ability to absorb light across a broad spectrum has led to its investigation in photovoltaic applications. Researchers have reported enhanced performance in organic solar cells when incorporating 4-IodoBenzenethiol as an active layer material.

In addition to its technical applications, 4-IodoBenzenethiol has gained attention for its role in fundamental chemical research. Its reactivity under various conditions provides insights into sulfur chemistry and aromatic substitution mechanisms. Recent experiments have utilized 4-IodoBenzenethiol to study intermolecular interactions, shedding light on supramolecular chemistry principles.

The environmental impact of 4-IodoBenzenethiol is another area of growing interest. Researchers are investigating its biodegradability and toxicity profiles to ensure sustainable use in industrial applications. Preliminary findings suggest that the compound exhibits moderate biodegradability under aerobic conditions, though further studies are needed to confirm its long-term environmental effects.

In conclusion, 4-IodoBenzenethiol (CAS No 52928-01-5) stands out as a multifaceted compound with diverse applications across multiple scientific disciplines. Its unique chemical properties, coupled with recent advancements in synthesis and application techniques, position it as a key molecule for future innovations in materials science, electronics, and biotechnology.

52928-01-5 (4-iodobenzene-1-thiol) Related Products

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Amadis Chemical Company Limited
(CAS:52928-01-5)4-iodobenzene-1-thiol
A1163874
Purity:99%/99%
Quantity:250.0mg/1.0g
Price ($):251.0/752.0
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