Cas no 1111120-02-5 (4-(4-Chloro-2-methylphenyl)-2-formylphenol)

4-(4-Chloro-2-methylphenyl)-2-formylphenol is a substituted phenolic compound featuring both chloro and formyl functional groups, making it a versatile intermediate in organic synthesis. Its molecular structure, incorporating a chloromethylphenyl moiety and a formylphenol group, lends itself to applications in pharmaceuticals, agrochemicals, and specialty chemical production. The compound’s reactivity allows for further functionalization, enabling the synthesis of complex derivatives. Its stability under standard conditions ensures consistent performance in synthetic workflows. The presence of both electron-withdrawing and electron-donating substituents enhances its utility in cross-coupling reactions and other transformations. This compound is particularly valuable in research and industrial settings requiring precise molecular modifications.
4-(4-Chloro-2-methylphenyl)-2-formylphenol structure
1111120-02-5 structure
Product Name:4-(4-Chloro-2-methylphenyl)-2-formylphenol
CAS No:1111120-02-5
MF:C14H11ClO2
MW:246.688943147659
MDL:MFCD11870920
CID:2620666
PubChem ID:53220460
Update Time:2025-11-02

4-(4-Chloro-2-methylphenyl)-2-formylphenol Chemical and Physical Properties

Names and Identifiers

    • MFCD11870920
    • 1111120-02-5
    • DTXSID20685196
    • 4-(4-CHLORO-2-METHYLPHENYL)-2-FORMYLPHENOL
    • 4-(4-Chloro-2-methylphenyl)-2-formylphenol, 95%
    • 4'-Chloro-4-hydroxy-2'-methyl[1,1'-biphenyl]-3-carbaldehyde
    • 4-(4-Chloro-2-methylphenyl)-2-formylphenol
    • MDL: MFCD11870920
    • Inchi: 1S/C14H11ClO2/c1-9-6-12(15)3-4-13(9)10-2-5-14(17)11(7-10)8-16/h2-8,17H,1H3
    • InChI Key: UADAKFFGRJRILQ-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=C(C)C=1)C1C=CC(=C(C=O)C=1)O

Computed Properties

  • Exact Mass: 246.0447573Da
  • Monoisotopic Mass: 246.0447573Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 2
  • Complexity: 269
  • 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: 4.2
  • Topological Polar Surface Area: 37.3?2

4-(4-Chloro-2-methylphenyl)-2-formylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB320872-5 g
4-(4-Chloro-2-methylphenyl)-2-formylphenol, 95%; .
1111120-02-5 95%
5 g
€1,159.00 2023-07-19
abcr
AB320872-5g
4-(4-Chloro-2-methylphenyl)-2-formylphenol, 95%; .
1111120-02-5 95%
5g
€1159.00 2025-04-22

Additional information on 4-(4-Chloro-2-methylphenyl)-2-formylphenol

4-(4-Chloro-2-methylphenyl)-2-formylphenol (CAS No. 1111120-02-5): A Comprehensive Overview

4-(4-Chloro-2-methylphenyl)-2-formylphenol (CAS No. 1111120-02-5) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, material science, and specialty chemical applications. This compound, characterized by its unique phenolic and formyl functional groups, exhibits properties that make it valuable for a range of industrial and research purposes. In this article, we delve into its chemical properties, applications, and the latest trends surrounding its use.

The molecular structure of 4-(4-Chloro-2-methylphenyl)-2-formylphenol includes a chloro-substituted phenyl ring and a formyl group attached to a phenol moiety. This configuration contributes to its reactivity and versatility in synthetic chemistry. Researchers often explore its potential as an intermediate in the synthesis of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its CAS No. 1111120-02-5 is frequently searched in scientific databases, reflecting its relevance in contemporary research.

One of the most discussed applications of 4-(4-Chloro-2-methylphenyl)-2-formylphenol is its role in the development of antimicrobial agents. With the global rise in antibiotic resistance, scientists are increasingly investigating novel compounds that can combat resistant strains. This compound's structural features make it a promising candidate for such studies. Additionally, its formyl group allows for further functionalization, enabling the creation of derivatives with tailored properties.

In the realm of material science, 4-(4-Chloro-2-methylphenyl)-2-formylphenol is explored for its potential in polymer synthesis. Its phenolic group can participate in polymerization reactions, leading to materials with enhanced thermal stability and mechanical strength. This aligns with the growing demand for high-performance polymers in industries such as automotive, aerospace, and electronics. Searches for phenolic polymers and advanced materials often intersect with discussions about this compound.

The market dynamics for 4-(4-Chloro-2-methylphenyl)-2-formylphenol are influenced by its niche applications. While not a bulk chemical, its specialty status ensures steady demand from research institutions and high-tech industries. Recent trends indicate a surge in interest from the Asia-Pacific region, where pharmaceutical and material science sectors are expanding rapidly. Companies specializing in fine chemicals are increasingly listing CAS No. 1111120-02-5 in their portfolios to cater to this demand.

Environmental and safety considerations are also critical when handling 4-(4-Chloro-2-methylphenyl)-2-formylphenol. Although it is not classified as a hazardous material under most regulatory frameworks, proper storage and handling protocols are essential to ensure safety. Researchers and manufacturers must adhere to guidelines to minimize any potential risks associated with its use. This aspect is frequently highlighted in safety data sheets and regulatory documents.

Looking ahead, the future of 4-(4-Chloro-2-methylphenyl)-2-formylphenol appears promising. Advances in synthetic methodologies and the increasing need for specialized intermediates in drug discovery are likely to drive its demand. Furthermore, its potential applications in green chemistry and sustainable materials align with global efforts to reduce environmental impact. As such, this compound is poised to remain a topic of interest in both academic and industrial circles.

In conclusion, 4-(4-Chloro-2-methylphenyl)-2-formylphenol (CAS No. 1111120-02-5) is a multifaceted compound with significant potential across various scientific disciplines. Its unique chemical properties, coupled with its applications in pharmaceuticals and materials science, make it a valuable asset for researchers and industries alike. By staying abreast of the latest developments and market trends, stakeholders can fully leverage the opportunities presented by this remarkable compound.

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