Date published: 2025-10-18

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2-Methylresorcinol (CAS 608-25-3)

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Application:
2-Methylresorcinol is a compound used in the synthesis of aromatic benziporphyrins
CAS Number:
608-25-3
Purity:
≥99%
Molecular Weight:
124.14
Molecular Formula:
C7H8O2
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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2-Methylresorcinol is an aromatic compound with a phenolic group. It is believed to interact with proteins and other biological molecules through hydrogen bonding and electrostatic interactions. It may act to interact with amino acid residues in proteins, and to form complexes with DNA. It is also believed to interact with enzymes and other proteins involved in signal transduction pathways, as well as proteins involved in transcriptional regulation.


2-Methylresorcinol (CAS 608-25-3) References

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  2. Rhodol Derivatives as Selective Fluorescent Probes for the Detection of HgII Ions and the Bioimaging of Hypochlorous Acid.  |  Li, L., et al. 2018. ChemistryOpen. 7: 136-143. PMID: 29435399
  3. Chemoenzymatic Total Synthesis of Sorbicatechol Structural Analogues and Evaluation of Their Antiviral Potential.  |  Sib, A., et al. 2020. Chembiochem. 21: 492-495. PMID: 31448469
  4. Reactions of Aminoacetals with C-Nucleophiles as a New Method for the Synthesis of Di(het)arylmethane Derivatives with a Taurine Fragment.  |  Smolobochkin, AV., et al. 2022. Russ J Gen Chem. 92: 161-165. PMID: 35308085
  5. 9-Trifluoromethylxanthenediols: Synthesis and Supramolecular Motifs.  |  Rodríguez-Molina, M., et al. 2022. ACS Omega. 7: 13520-13528. PMID: 35559143
  6. Design, Synthesis, and Antifungal Activity of 4-Amino Coumarin Based Derivatives.  |  Xu, L., et al. 2022. Molecules. 27: PMID: 35566096
  7. Chemicals of concern in personal care products used by women of color in three communities of California.  |  Johnson, PI., et al. 2022. J Expo Sci Environ Epidemiol. 32: 864-876. PMID: 36323919
  8. Expansion of the application domain of a macromolecular ocular irritation test (OptiSafe™).  |  Lebrun, S., et al. 2023. Toxicol In Vitro. 86: 105515. PMID: 36351539
  9. Bioactive Compounds, Pharmacological Actions, and Pharmacokinetics of Genus Acacia.  |  Batiha, GE., et al. 2022. Molecules. 27: PMID: 36364163
  10. Synthesis of Novel Cavitand Host Molecules via Palladium-Catalyzed Aryloxy- and Azidocarbonylation.  |  Akash, ., et al. 2022. Molecules. 27: PMID: 36500499
  11. Heterocyclic Synthesis of Crowded Aposafranones: Structure of 1-Methyl-8-dimethylamino-10-phenylphenazin-2-(10H)one and Related Compounds.  |  Plater, MJ. and Harrison, WTA. 2023. ChemistryOpen. 12: e202300007. PMID: 36782392
  12. Utilization of vanillin to prepare sulfated Calix[4]resorcinarene as efficient organocatalyst for biodiesel production based on methylation of palmitic acid and oleic acid.  |  Jumina, J., et al. 2023. Heliyon. 9: e16100. PMID: 37251819
  13. Control of Bandgaps and Energy Levels in Water-Soluble Discontinuously Conjugated Polymers through Chemical Modification.  |  Guo, HX., et al. 2023. Polymers (Basel). 15: PMID: 37376384

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Methylresorcinol, 100 g

sc-256209
100 g
$49.00