Date published: 2025-11-12

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Anisole (CAS 100-66-3)

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Application:
Anisole is a biochemical for proteomics research
CAS Number:
100-66-3
Purity:
≥98%
Molecular Weight:
108.14
Molecular Formula:
C7H8O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Anisole is a compound employed in organic chemistry research due to its role as a versatile precursor and solvent in synthesis processes. Its methoxy group makes it a subject of interest in studies involving nucleophilic substitution reactions where anisole can act as an electrophile. Research involving anisole often aims to understand the influence of methoxy substitution on the reactivity of aromatic systems. Moreover, anisole is used in the synthesis of a wide range of chemical products, including fragrances, dyes, and pharmaceuticals, by exploiting its ability to undergo electrophilic aromatic substitution. Additionally, due to its electron-donating properties, anisole is often utilized in studies that require the stabilization of positive charge or the enhancement of base strength in a reaction intermediate.


Anisole (CAS 100-66-3) References

  1. Anisole at 100 K: the first crystal structure determination.  |  Seidel, RW. and Goddard, R. 2015. Acta Crystallogr C Struct Chem. 71: 664-6. PMID: 26243411
  2. Spectroscopic Properties of Anisole at the Air-Ice Interface: A Combined Experimental-Computational Approach.  |  Malongwe, JK., et al. 2016. Langmuir. 32: 5755-64. PMID: 27243785
  3. Electron-Beam Patterning of Vapor-Deposited Solid Anisole.  |  Zhao, D., et al. 2020. ACS Appl Mater Interfaces. 12: 6436-6441. PMID: 31942796
  4. Anisole-modified hyper-cross-linked resins for efficient adsorption of aniline from aqueous solution.  |  Zeng, X. and Huang, J. 2020. J Colloid Interface Sci. 569: 177-183. PMID: 32113015
  5. Atmospheric Hydrodeoxygenation of Anisole to Hydrocarbons Over Ni Supported on Mesoporous Silica.  |  Lee, H., et al. 2020. J Nanosci Nanotechnol. 20: 5734-5737. PMID: 32331169
  6. Metal-Acid Synergy: Hydrodeoxygenation of Anisole over Pt/Al-SBA-15.  |  Shivhare, A., et al. 2020. ChemSusChem. 13: 4945-4953. PMID: 32449298
  7. Safety of butylated hydroxy anisole (BHA) for all animal species.  |  , ., et al. 2019. EFSA J. 17: e05913. PMID: 32626203
  8. Partitioning of Selected Anisole and Veratrole Derivatives between Water and Anionic Surfactant Micelles.  |  Lewandowski, A. and Szymczyk, K. 2020. Molecules. 25: PMID: 33317196
  9. Acylation of Anisole With Benzoyl Chloride Over Rapidly Synthesized Fly Ash-Based HBEA Zeolite.  |  Ameh, AE., et al. 2021. Front Chem. 9: 683125. PMID: 34222196
  10. Theoretical Study of O-CH3 Bond Dissociation Enthalpy in Anisole Systems.  |  Li, R., et al. 2021. ACS Omega. 6: 21952-21959. PMID: 34497890
  11. Bimetallic Niobium-Based Catalysts Supported on SBA-15 for Hydrodeoxygenation of Anisole.  |  Ballesteros-Plata, D., et al. 2021. Ind Eng Chem Res. 60: 18831-18840. PMID: 35264821
  12. Secondary organic aerosol formation from atmospheric reactions of anisole and associated health effects.  |  Li, C., et al. 2022. Chemosphere. 308: 136421. PMID: 36108757
  13. Anisole hydrodeoxygenation over Ni-Co bimetallic catalyst: a combination of experimental, kinetic and DFT study.  |  Kumar, A., et al. 2022. RSC Adv. 12: 30236-30247. PMID: 36337943

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Anisole, 500 ml

sc-233877
500 ml
$65.00

Anisole, 2.5 L

sc-233877A
2.5 L
$204.00