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5-Amino-3-phenyl-1,2,4-thiadiazole (CAS 17467-15-1)

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Alternate Names:
3-phenyl-1,2,4-thiadiazol-5-amine
CAS Number:
17467-15-1
Molecular Weight:
177.23
Molecular Formula:
C8H7N3S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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5-Amino-3-phenyl-1,2,4-thiadiazole is a significant organic compound extensively employed in diverse scientific research domains. 5-Amino-3-phenyl-1,2,4-thiadiazole has found extensive use in scientific research applications due to its remarkable reactivity and stability. It has been employed in synthesizing various heterocyclic compounds, including derivatives of 1,2,4-triazol-3-yl-phenyl and 2-aryl-5-aminothiadiazoles. Additionally, the compound has been utilized in synthesizing organic compounds such as derivatives of 5-amino-1,2,4-thiadiazole-3-phenyl and 5-amino-1,2,4-thiadiazol-3-phenyl-3-methyl. It has further found application in the synthesis of polymers like poly(5-Amino-3-phenyl-1,2,4-thiadiazole). Furthermore, 5-Amino-3-phenyl-1,2,4-thiadiazole acts as an inhibitor of cyclooxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX). Additionally, the compound inhibits the release of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) and interleukin-1β (IL-1β).


5-Amino-3-phenyl-1,2,4-thiadiazole (CAS 17467-15-1) References

  1. Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists.  |  van Muijlwijk-Koezen, JE., et al. 2001. J Med Chem. 44: 749-62. PMID: 11262085
  2. Novel antiallergic and antiinflammatory agents. Part I: Synthesis and pharmacology of glycolic amide derivatives.  |  Ban, M., et al. 1998. Bioorg Med Chem. 6: 1069-76. PMID: 9730244
  3. Rates of reversible bond switch with participation of. pi.-bonded sulfur (IV) in a protonated thiadiazole ring system  |  Yamamoto, Y., & Akiba, K. Y. 1984. Journal of the American Chemical Society. 106(9): 2713-2715.
  4. Colour and constitution of some N-phenylpyrrolidinylazo dyes: application of the PPP molecular orbital method  |  Hallas, G., & Marsden, R. 1985. Dyes and pigments. 6(6): 463-475.
  5. Studies of heterocyclic compounds. Part 31. 4-Alkyl-5-alkylimino-Δ 2-1, 2, 4-thiadiazolines: synthesis and cycloaddition reactions with nitriles in attempts to prepare 3aλ 4-thia-1, 3, 4, 6-tetraazapentalenes  |  Lai, L. L., Ngoi, T. H., Reid, D. H., Nicol, R. H., & Rhodes, J. B. 1993. Journal of the Chemical Society, Perkin Transactions 1. (15): 1753-1759.
  6. One‐Pot Synthesis of 3‐Aryl‐5‐amino‐1, 2, 4‐thiadiazoles from Imidates and Thioureas by I2‐Mediated Oxidative Construction of the N–S Bond  |  Chai, L., Lai, Z., Xia, Q., Yuan, J., Bian, Q., Yu, M.,.. & Xu, H. 2018. European Journal of Organic Chemistry. 2018(31): 4338-4344.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Amino-3-phenyl-1,2,4-thiadiazole, 1 g

sc-281446
1 g
$143.00