Date published: 2026-1-6

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1-Benzoyl-3-phenyl-2-thiourea (CAS 4921-82-8)

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Alternate Names:
N-[(Phenylamino)thioxomethyl]-benzamide
CAS Number:
4921-82-8
Molecular Weight:
256.32
Molecular Formula:
C14H12N2OS
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-Benzoyl-3-phenyl-2-thiourea (BPTU) is a synthetic compound with a multitude of applications. 1-Benzoyl-3-phenyl-2-thiourea possesses a unique structure and possesses properties that render it highly suitable for a wide array of applications. In the realm of scientific research, 1-Benzoyl-3-phenyl-2-thiourea demonstrates its versatility and utility. It finds application in the synthesis of polymers and nanomaterials. Furthermore, 1-Benzoyl-3-phenyl-2-thiourea plays a role in synthesizing peptides and other bioactive molecules. While the precise mechanism of action of 1-Benzoyl-3-phenyl-2-thiourea remains incompletely understood, it is postulated that this compound acts as a nucleophile, readily engaging with electrophilic compounds to form stable covalent bonds. Additionally, 1-Benzoyl-3-phenyl-2-thiourea exhibits the ability to form complexes with other molecules.


1-Benzoyl-3-phenyl-2-thiourea (CAS 4921-82-8) References

  1. Valproic acid inhibits glioblastoma multiforme cell growth via paraoxonase 2 expression.  |  Tseng, JH., et al. 2017. Oncotarget. 8: 14666-14679. PMID: 28108734
  2. HDAC8 Prevents Anthrax Lethal Toxin-induced Cell Cycle Arrest through Silencing PTEN in Human Monocytic THP-1 Cells.  |  Ha, SD., et al. 2017. Toxins (Basel). 9: PMID: 28509866
  3. Histone deacetylase 8 protects human proximal tubular epithelial cells from hypoxia-mimetic cobalt- and hypoxia/reoxygenation-induced mitochondrial fission and cytotoxicity.  |  Ha, SD., et al. 2018. Sci Rep. 8: 11332. PMID: 30054507

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Benzoyl-3-phenyl-2-thiourea, 1 g

sc-258614A
1 g
$43.00

1-Benzoyl-3-phenyl-2-thiourea, 5 g

sc-258614
5 g
$129.00