Date published: 2026-2-8

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4-(Dimethylamino)benzoyl chloride (CAS 4755-50-4)

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Alternate Names:
DMABC
CAS Number:
4755-50-4
Purity:
97%
Molecular Weight:
183.63
Molecular Formula:
C9H10ClNO
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-(Dimethylamino)benzoyl chloride is a chemical compound that functions as an acylating agent in organic synthesis. It is used to introduce the 4-(dimethylamino)benzoyl group into various organic molecules, allowing for the modification of their chemical properties. The mechanism of action of 4-(Dimethylamino)benzoyl chloride involves the acylation of nucleophilic functional groups, such as amines and alcohols, through the formation of an amide or ester bond. 4-(Dimethylamino)Benzoyl Chloride reaction occurs through the displacement of the chloride ion by the nucleophile, resulting in the formation of the desired acylated product. In this way, 4-(Dimethylamino)benzoyl chloride serves versatile for the modification of organic molecules in development applications, allowing for the synthesis of new compounds with tailored properties.


4-(Dimethylamino)benzoyl chloride (CAS 4755-50-4) References

  1. 7.87 eV laser desorption postionization mass spectrometry of adsorbed and covalently bound bisphenol A diglycidyl methacrylate.  |  Zhou, M., et al. 2007. J Am Soc Mass Spectrom. 18: 1097-108. PMID: 17449273
  2. Synthesis of lipophilic 1-deoxygalactonojirimycin derivatives as D-galactosidase inhibitors.  |  Schitter, G., et al. 2010. Beilstein J Org Chem. 6: 21. PMID: 20502610
  3. From COX-2 inhibitor nimesulide to potent anti-cancer agent: synthesis, in vitro, in vivo and pharmacokinetic evaluation.  |  Zhong, B., et al. 2012. Eur J Med Chem. 47: 432-444. PMID: 22119125
  4. Synthesis, biological evaluation, and structure-activity relationships of N-benzoyl-2-hydroxybenzamides as agents active against P. falciparum (K1 strain), Trypanosomes, and Leishmania.  |  Stec, J., et al. 2012. J Med Chem. 55: 3088-100. PMID: 22352841
  5. Optimization of a small tropomyosin-related kinase B (TrkB) agonist 7,8-dihydroxyflavone active in mouse models of depression.  |  Liu, X., et al. 2012. J Med Chem. 55: 8524-37. PMID: 22984948
  6. O-methylated metabolite of 7,8-dihydroxyflavone activates TrkB receptor and displays antidepressant activity.  |  Liu, X., et al. 2013. Pharmacology. 91: 185-200. PMID: 23445871
  7. MetFish: a Metabolomics Pipeline for Studying Microbial Communities in Chemically Extreme Environments.  |  Xu, C., et al. 2021. mSystems. 6: e0105820. PMID: 34061574
  8. The Uptake of Sporopollenin Exine Capsules and Associated Bioavailability of Adsorbed Oestradiol in Selected Aquatic Invertebrates.  |  Chapman, E., et al. 2021. Bull Environ Contam Toxicol. 107: 876-882. PMID: 34459949
  9. Ruthenium Olefin Metathesis Catalysts Featuring N-Heterocyclic Carbene Ligands Tagged with Isonicotinic and 4-(Dimethylamino)benzoic Acid Rests: Evaluation of a Modular Synthetic Strategy.  |  Czarnocki, S., et al. 2021. Molecules. 26: PMID: 34500654
  10. Qualitative Determination of Polysulfide Species in a Lithium-Sulfur Battery by HR-LC-APCI-MSn with One-Step Derivatization.  |  Kim, SY., et al. 2022. J Am Soc Mass Spectrom. 33: 1653-1658. PMID: 35905433

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-(Dimethylamino)benzoyl chloride, 1 g

sc-252097
1 g
$51.00