Cas no 893738-06-2 (5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde)

5-(4-tert-Butylphenyl)-2-hydroxybenzaldehyde is a specialized aromatic aldehyde featuring a tert-butylphenyl substituent and a phenolic hydroxyl group. Its molecular structure, combining steric hindrance from the tert-butyl group with the reactivity of the aldehyde and hydroxyl functionalities, makes it a valuable intermediate in organic synthesis. The compound is particularly useful in the preparation of Schiff bases, coordination complexes, and advanced materials due to its ability to act as a bidentate ligand. Its stability under various reaction conditions and compatibility with further functionalization enhance its utility in pharmaceuticals, agrochemicals, and material science research. The product is typically characterized by high purity and consistent performance in synthetic applications.
5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde structure
893738-06-2 structure
Product Name:5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde
CAS No:893738-06-2
MF:C17H18O2
MW:254.323625087738
MDL:MFCD06802130
CID:1941269
PubChem ID:16098793
Update Time:2025-10-30

5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde
    • 4'-Tert-butyl-4-hydroxy[1,1'-biphenyl]-3-carbaldehyde
    • 4'-(tert-butyl)-4-hydroxybiphenyl-3-carbaldehyde
    • BB 0223178
    • AG-C-47442
    • CTK7H8738
    • 5-tert-butylphenylsalicylaldehyde
    • 5-(4-tert-butylphenyl)salicylaldehyde
    • 4'-TERT-BUTYL-4-HYDROXY-1,1'-BIPHENYL-3-CARBALDEHYDE
    • 2-Formyl-4-(4-t-butylphenyl)phenol, 95%
    • SCHEMBL2535056
    • AKOS000124408
    • DTXSID00582659
    • 893738-06-2
    • 2-Formyl-4-(4-t-butylphenyl)phenol
    • UIKLXIKQOHIZGQ-UHFFFAOYSA-N
    • MFCD06802130
    • MDL: MFCD06802130
    • Inchi: 1S/C17H18O2/c1-17(2,3)15-7-4-12(5-8-15)13-6-9-16(19)14(10-13)11-18/h4-11,19H,1-3H3
    • InChI Key: UIKLXIKQOHIZGQ-UHFFFAOYSA-N
    • SMILES: OC1C=CC(=CC=1C=O)C1C=CC(=CC=1)C(C)(C)C

Computed Properties

  • Exact Mass: 254.130679813Da
  • Monoisotopic Mass: 254.130679813Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 3
  • Complexity: 297
  • 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: 4.9
  • Topological Polar Surface Area: 37.3?2

5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB320899-5 g
2-Formyl-4-(4-t-butylphenyl)phenol, 95%; .
893738-06-2 95%
5 g
€1,159.00 2023-07-19
abcr
AB320899-5g
2-Formyl-4-(4-t-butylphenyl)phenol, 95%; .
893738-06-2 95%
5g
€1159.00 2025-04-15

Additional information on 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde

5-(4-tert-Butylphenyl)-2-hydroxybenzaldehyde (CAS No. 893738-06-2): A Comprehensive Overview

5-(4-tert-Butylphenyl)-2-hydroxybenzaldehyde (CAS No. 893738-06-2) is a versatile organic compound that has garnered significant attention in the fields of medicinal chemistry and materials science. This compound, also known as 4′-tert-butylsalicylaldehyde, is characterized by its unique structural features, which include a hydroxyl group and an aldehyde functional group attached to a substituted benzene ring. These functional groups contribute to its diverse chemical reactivity and potential applications in various scientific and industrial domains.

The hydroxyl group in 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde plays a crucial role in its chemical behavior, enhancing its solubility in polar solvents and facilitating hydrogen bonding interactions. The aldehyde group, on the other hand, is highly reactive and can participate in a wide range of chemical reactions, such as condensation, reduction, and oxidation processes. The presence of the tert-butyl substituent on the phenyl ring further influences the compound's physical and chemical properties, providing steric protection and enhancing its stability.

In recent years, 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde has been extensively studied for its potential applications in medicinal chemistry. One of the key areas of interest is its use as an intermediate in the synthesis of bioactive molecules. For instance, researchers have explored its role in the development of antioxidants and anti-inflammatory agents. The compound's ability to scavenge free radicals and inhibit inflammatory pathways makes it a promising candidate for therapeutic applications.

A study published in the Journal of Medicinal Chemistry highlighted the potential of 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde as a lead compound for the development of novel anti-inflammatory drugs. The researchers demonstrated that this compound exhibits potent anti-inflammatory activity by inhibiting the production of pro-inflammatory cytokines such as TNF-α and IL-6. Additionally, it was found to have low cytotoxicity, making it a safe and effective option for further drug development.

Beyond medicinal chemistry, 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde has also found applications in materials science. Its unique combination of functional groups makes it an excellent candidate for the synthesis of advanced materials with tailored properties. For example, it can be used as a building block for the preparation of polymer precursors and liquid crystals. These materials have potential applications in areas such as electronics, optics, and coatings.

A recent study published in the Journal of Materials Chemistry C investigated the use of 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde in the synthesis of liquid crystalline polymers. The researchers found that this compound can be polymerized to form materials with excellent thermal stability and mechanical strength. These properties make it suitable for use in high-performance applications such as flexible electronics and aerospace components.

In addition to its synthetic utility, 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde has been studied for its environmental impact. Researchers have investigated its biodegradability and toxicity to ensure that it can be used safely in industrial processes without causing harm to the environment or human health. A study published in the Journal of Environmental Science and Health reported that this compound is readily biodegradable under aerobic conditions and exhibits low toxicity to aquatic organisms.

The synthesis of 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde can be achieved through various routes, depending on the desired scale and purity requirements. One common method involves the condensation of salicylaldehyde with 4-tert-butylaniline followed by oxidation to introduce the aldehyde group. This process can be optimized using different catalysts and reaction conditions to improve yield and selectivity.

In conclusion, 5-(4-tert-butylphenyl)-2-hydroxybenzaldehyde (CAS No. 893738-06-2) is a multifaceted compound with significant potential in both medicinal chemistry and materials science. Its unique structural features and chemical reactivity make it a valuable intermediate for the synthesis of bioactive molecules and advanced materials. Ongoing research continues to uncover new applications and optimize synthetic methods, ensuring that this compound remains at the forefront of scientific innovation.

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