Cas no 40463-26-1 (5-(3-Methoxyphenyl)-2-methyl-1-pentene)

5-(3-Methoxyphenyl)-2-methyl-1-pentene structure
40463-26-1 structure
Product Name:5-(3-Methoxyphenyl)-2-methyl-1-pentene
CAS No:40463-26-1
MF:C13H18O
MW:190.281424045563
MDL:MFCD11554049
CID:2667537
Update Time:2025-04-23

5-(3-Methoxyphenyl)-2-methyl-1-pentene Chemical and Physical Properties

Names and Identifiers

    • 1-Methoxy-3-(4-methyl-4-pentenyl)benzene
    • 5-(3-Methoxyphenyl)-2-methyl-1-pentene
    • 1-methoxy-3-(4-methylpent-4-enyl)benzene
    • Benzene, 1-methoxy-3-(4-methyl-4-pentenyl)-
    • HWJRHUZDQWESQU-UHFFFAOYSA-N
    • 1-Methoxy-3-(4-methyl-4-pentenyl)benzene #
    • MDL: MFCD11554049
    • Inchi: 1S/C13H18O/c1-11(2)6-4-7-12-8-5-9-13(10-12)14-3/h5,8-10H,1,4,6-7H2,2-3H3
    • InChI Key: HWJRHUZDQWESQU-UHFFFAOYSA-N
    • SMILES: O(C)C1=CC=CC(=C1)CCCC(=C)C

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 174
  • XLogP3: 4.8
  • Topological Polar Surface Area: 9.2

5-(3-Methoxyphenyl)-2-methyl-1-pentene Pricemore >>

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Additional information on 5-(3-Methoxyphenyl)-2-methyl-1-pentene

5-(3-Methoxyphenyl)-2-methyl-1-pentene: A Comprehensive Overview

5-(3-Methoxyphenyl)-2-methyl-1-pentene (CAS No. 40463-26-1) is a versatile organic compound that has garnered significant attention in the fields of organic chemistry, materials science, and pharmacology. This compound, characterized by its unique structure and properties, has been the subject of extensive research in recent years. Its applications span across various industries, making it a valuable molecule in modern chemical synthesis.

The molecular structure of 5-(3-Methoxyphenyl)-2-methyl-1-pentene is defined by a conjugated system that includes a methoxy-substituted phenyl group and a methyl-substituted pentene chain. This combination imparts the compound with distinctive electronic and steric properties, which are crucial for its functional applications. The methoxyphenyl group contributes to the compound's aromaticity and electron-donating capabilities, while the methyl-substituted pentene chain enhances its hydrophobicity and flexibility.

Recent studies have highlighted the potential of 5-(3-Methoxyphenyl)-2-methyl-1-pentene in the development of advanced materials. For instance, researchers have explored its use as a precursor for synthesizing conjugated polymers, which are widely used in organic electronics. The compound's ability to undergo polymerization under controlled conditions has made it a valuable building block for creating materials with tailored electronic properties.

In addition to its role in materials science, 5-(3-Methoxyphenyl)-2-methyl-1-pentene has also been investigated for its pharmacological applications. Preclinical studies suggest that this compound exhibits promising bioactivity, particularly in modulating cellular signaling pathways associated with inflammation and oxidative stress. Its methoxyphenyl moiety is believed to play a critical role in these biological effects, as it is known to interact with various protein targets.

The synthesis of 5-(3-Methoxyphenyl)-2-methyl-1-pentene typically involves a multi-step process that combines principles from organic synthesis and catalysis. Recent advancements in catalytic methods have enabled more efficient and selective routes to this compound, reducing production costs and improving yields. These developments have made the compound more accessible for both academic research and industrial applications.

From an environmental perspective, the ecological impact of 5-(3-Methoxyphenyl)-2-methyl-1-pentene has been a topic of interest. Studies have shown that the compound exhibits moderate biodegradability under aerobic conditions, suggesting that it poses minimal long-term risks to ecosystems when properly managed. However, further research is needed to fully understand its environmental fate and toxicity profiles.

In conclusion, 5-(3-Methoxyphenyl)-2-methyl-1-pentene (CAS No. 40463-26-1) is a multifaceted organic compound with significant potential across diverse fields. Its unique chemical properties, coupled with recent advances in synthesis and application development, position it as a key molecule for future innovations in materials science and pharmacology.

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