Cas no 1261898-71-8 (4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol)

4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol is a specialized aromatic compound featuring both formyl and methoxycarbonyl functional groups, making it a versatile intermediate in organic synthesis. Its unique structure allows for selective reactivity in cross-coupling reactions, cyclizations, and other transformations, particularly in pharmaceutical and agrochemical applications. The chloro substituent enhances its utility as a precursor for further functionalization, while the phenol group offers additional derivatization opportunities. This compound is valued for its stability under standard conditions and compatibility with a range of reaction conditions. Its well-defined molecular architecture makes it suitable for constructing complex heterocyclic frameworks or fine-tuning bioactive molecules in research and industrial settings.
4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol structure
1261898-71-8 structure
Product Name:4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol
CAS No:1261898-71-8
MF:C15H11ClO4
MW:290.698443651199
MDL:MFCD18314878
CID:2762104
PubChem ID:53220624
Update Time:2025-06-08

4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol Chemical and Physical Properties

Names and Identifiers

    • 1261898-71-8
    • 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol, 95%
    • 4-(2-CHLORO-5-METHOXYCARBONYLPHENYL)-2-FORMYLPHENOL
    • DTXSID80685354
    • Methyl 6-chloro-3'-formyl-4'-hydroxy[1,1'-biphenyl]-3-carboxylate
    • MFCD18314878
    • 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol
    • MDL： MFCD18314878
    • Inchi： 1S/C15H11ClO4/c1-20-15(19)10-2-4-13(16)12(7-10)9-3-5-14(18)11(6-9)8-17/h2-8,18H,1H3
    • InChI Key： CPIMILXLFNRQFB-UHFFFAOYSA-N
    • SMILES： ClC1=CC=C(C(=O)OC)C=C1C1C=CC(=C(C=O)C=1)O

Computed Properties

  • Exact Mass: 290.0345865Da
  • Monoisotopic Mass: 290.0345865Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 4
  • Complexity: 360
  • 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: 63.6?2

4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB321052-5 g
4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol, 95%; .
 1261898-71-8 95%
5g
 €1159.00 2023-04-26
abcr
AB321052-5g
4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol, 95%; .
 1261898-71-8 95%
5g
 €1159.00 2025-02-21

4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol Related Literature

Additional information on 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol

Comprehensive Overview of 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261898-71-8)

4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261898-71-8) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, material science, and synthetic chemistry. This compound, characterized by its unique chloro and methoxycarbonyl functional groups, serves as a versatile intermediate in the synthesis of complex molecules. Its molecular structure, featuring a phenol core with a formyl substituent, makes it a valuable building block for designing advanced materials and bioactive agents.

In recent years, the demand for 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol has surged due to its potential applications in drug discovery and development. Researchers are particularly interested in its role as a precursor for heterocyclic compounds, which are pivotal in creating new therapeutics for diseases such as cancer and neurodegenerative disorders. The compound's chloro group enhances its reactivity, enabling selective modifications that are crucial for tailoring its properties to specific applications.

The synthesis of CAS No. 1261898-71-8 involves multi-step organic reactions, including Friedel-Crafts acylation and Vilsmeier-Haack formylation, which are well-documented in the literature. These methods ensure high purity and yield, making the compound a reliable choice for industrial and academic laboratories. Its methoxycarbonyl moiety further contributes to its stability, allowing for long-term storage and handling under standard conditions.

One of the most frequently asked questions about 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol revolves around its solubility and compatibility with common solvents. Studies indicate that it is soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) and methanol, which facilitates its use in various chemical reactions. This property is particularly advantageous for researchers working on high-throughput screening and combinatorial chemistry, where solubility is a critical factor.

From an environmental and safety perspective, CAS No. 1261898-71-8 is classified as a low-toxicity compound, provided it is handled with standard laboratory precautions. Its phenol derivative nature necessitates proper ventilation and personal protective equipment (PPE) to minimize exposure. However, it does not fall under the category of hazardous materials, making it a safer alternative compared to other reactive intermediates.

The growing interest in sustainable chemistry has also highlighted the potential of 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol in green synthesis. Its ability to participate in catalytic reactions and biodegradable pathways aligns with the global shift toward eco-friendly chemical processes. This aspect is particularly relevant to industries aiming to reduce their carbon footprint while maintaining high efficiency in production.

In conclusion, 4-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261898-71-8) stands out as a multifunctional compound with broad applications in modern chemistry. Its unique structural features, combined with its reactivity and safety profile, make it a valuable asset for researchers and manufacturers alike. As the scientific community continues to explore its potential, this compound is poised to play a pivotal role in advancing both pharmaceutical innovations and sustainable material development.

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