Date published: 2025-11-20

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4-(Methylthio)benzaldehyde (CAS 3446-89-7)

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Alternate Names:
4-(Methylmercapto)benzaldehyde
CAS Number:
3446-89-7
Molecular Weight:
152.21
Molecular Formula:
C8H8OS
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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4-(Methylthio)benzaldehyde, known as 4-MTBA, is an aromatic aldehyde frequently employed in the synthesis of drugs and various compounds. This versatile compound serves as a intermediate in the production of several pharmaceuticals, including well-known anti-cancer drugs like paclitaxel and taxol. To obtain 4-(Methylthio)benzaldehyde, it is synthesized from 4-methylthiobenzene sulfoxide, which is derived from the reaction between 4-methylthiobenzene and sulfur trioxide. The synthesis involves the reaction of 4-methylthiobenzene sulfoxide with an aldehyde, like formaldehyde, under the influence of an acid catalyst such as sulfuric acid. Generally conducted at temperatures ranging from 40-60°C, this process is usually completed within 1-2 hours. 4-(Methylthio)benzaldehyde stands as a valuable and versatile compound, finding use in numerous applications across chemical industries. Its importance as an intermediate underscores its significance in modern scientific endeavors.


4-(Methylthio)benzaldehyde (CAS 3446-89-7) References

  1. Synthesis and pharmacological studies of new pyrazole analogues of podophyllotoxin.  |  Umesha, B. and Basavarajuk, YB. 2014. Bioorg Khim. 40: 503-12. PMID: 25898761
  2. Thiazolidin-4-ones from 4-(methylthio)benzaldehyde and 4-(methylsulfonyl)benzaldehyde: Synthesis, antiglioma activity and cytotoxicity.  |  da Silva, DS., et al. 2016. Eur J Med Chem. 124: 574-582. PMID: 27614406
  3. Quantitative surface-enhanced Raman spectroscopy for kinetic analysis of aldol condensation using Ag-Au core-shell nanocubes.  |  Weatherston, JD., et al. 2016. Analyst. 141: 6051-6060. PMID: 27747320
  4. One-pot cascade synthesis and in vitro evaluation of anti-inflammatory and antidiabetic activities of S-methylphenyl substituted acridine-1,8-diones.  |  Mallu, L., et al. 2017. Chem Biol Drug Des. 90: 520-526. PMID: 28294548

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-(Methylthio)benzaldehyde, 10 g

sc-232288
10 g
$46.00