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1,3,5-Trimethoxybenzene (CAS 621-23-8)

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Application:
1,3,5-Trimethoxybenzene is a compound that is predominant in the Chinese variety of roses
CAS Number:
621-23-8
Molecular Weight:
168.19
Molecular Formula:
C6H3(OCH3)3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,3,5-Trimethoxybenzene is a compound that functions as a precursor in the synthesis of various organic compounds. Its mechanism of action involves participating in chemical reactions as a starting material for the production of more complex molecules. Within the experimental, it serves as a building block for the creation of diverse chemical structures, contributing to the development of new materials and substances. At the molecular level, 1,3,5-Trimethoxybenzene undergoes reactions that lead to the formation of different derivatives, enabling the modification and enhancement of its chemical properties. Its role in development involves its participation in pathways, allowing for the generation of novel compounds with potential applications in various fields. 1,3,5-Trimethoxybenzene plays a functional role as a chemical precursor, contributing to the advancement of scientific knowledge and the creation of new chemical entities.


1,3,5-Trimethoxybenzene (CAS 621-23-8) References

  1. Biosynthesis of the major scent components 3,5-dimethoxytoluene and 1,3,5-trimethoxybenzene by novel rose O-methyltransferases.  |  Scalliet, G., et al. 2002. FEBS Lett. 523: 113-8. PMID: 12123815
  2. The key role of phloroglucinol O-methyltransferase in the biosynthesis of Rosa chinensis volatile 1,3,5-trimethoxybenzene.  |  Wu, S., et al. 2004. Plant Physiol. 135: 95-102. PMID: 15122041
  3. Two O-methyltransferases isolated from flower petals of Rosa chinensis var. spontanea involved in scent biosynthesis.  |  Wu, S., et al. 2003. J Biosci Bioeng. 96: 119-28. PMID: 16233496
  4. One-electron oxidation of alcohols by the 1,3,5-trimethoxybenzene radical cation in the excited state during two-color two-laser flash photolysis.  |  Cai, X., et al. 2007. J Phys Chem A. 111: 1788-91. PMID: 17295459
  5. Both the adaxial and abaxial epidermal layers of the rose petal emit volatile scent compounds.  |  Bergougnoux, V., et al. 2007. Planta. 226: 853-66. PMID: 17520281
  6. Leaf essential oil composition of three species of Myrcianthes from Monteverde, Costa Rica.  |  Cole, RA., et al. 2008. Chem Biodivers. 5: 1327-34. PMID: 18649320
  7. Ozonolysis of lignin models in aqueous solution: anisole, 1,2-dimethoxybenzene, 1,4-dimethoxybenzene, and 1,3,5-trimethoxybenzene.  |  Mvula, E., et al. 2009. Environ Sci Technol. 43: 6275-82. PMID: 19746725
  8. Trimethoxybenzene complexes of pentafluorophenylchlorocarbene.  |  Wang, L., et al. 2011. J Phys Chem A. 115: 8113-8. PMID: 21696161
  9. Practical N-Hydroxyphthalimide-Mediated Oxidation of Sulfonamides to N-Sulfonylimines.  |  Wang, J. and Yi, WJ. 2019. Molecules. 24: PMID: 31635092
  10. Chemical composition of hydrosol volatiles of flowers from ten Paeonia × suffruticosa Andr. cultivars from Luoyang, China.  |  Lei, G., et al. 2021. Nat Prod Res. 35: 3509-3513. PMID: 31928365
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  12. Hygroscopic Tendencies of Substances Used as Calibrants for Quantitative Nuclear Magnetic Resonance Spectroscopy.  |  Suiter, CL. and Widegren, JA. 2021. Anal Chem. 93: 16977-16980. PMID: 34898163
  13. Nucleosides and amino acids, isolated from Cordyceps sinensis, protected against cyclophosphamide-induced myelosuppression in mice.  |  Zhang, Y., et al. 2022. Nat Prod Res. 36: 6056-6059. PMID: 35188001
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,3,5-Trimethoxybenzene, 10 g

sc-223003
10 g
$29.00

1,3,5-Trimethoxybenzene, 50 g

sc-223003A
50 g
$92.00