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CS-W001157 4
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5-(tert-Butyl)-1,3,4-thiadiazol-2-amine

  • CAS No. 39222-73-6

  • Cat. No. CS-W010909
  • Molecule weight157.24
  • Purity≥97%
  • MDL No.MFCD00040403

*For research and further manufacturing use only, not for direct human use.

5-(tert-Butyl)-1,3,4-thiadiazol-2-amine|CS-W010909

Structure of 39222-73-6

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General Information

  • CAS No. 39222-73-6
  • Cat. No. CS-W010909
  • Purity ≥97%
  • MDL No. MFCD00040403
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₁₁N₃S
  • Molecular Weight 157.24
  • Synonym(s) Amino-5-tert-butyl-1,3,4-thiadiazole,2-
  • SMILES CC(C)(C)C1=NN=C(N)S1

Description

5-(tert-Butyl)-1,3,4-thiadiazol-2-amine features a sterically hindered tert-butyl group that enhances solubility and stability in organic media. The thiadiazole core delivers strong electron-withdrawing character, enabling effective integration into heterocyclic scaffolds for medicinal chemistry applications. This bench-stable compound serves as a key building block in the synthesis of bioactive molecules requiring nitrogen-rich, polarizable heterocycles.

Synthesis

  • Route1

    References

    • Hilfiker, Mark A.; Wang, Ning; Hou, Xiaoping; Du, Zhimin; Pullen, Mark A.; Nord, Melanie; Nagilla, Rakesh; Fries, Harvey E.; Wu, Charlene W.; Sulpizio, Anthony C.; Jaworski, Jon-Paul; Morrow, Dwight; Edwards, Richard M.; Jin, Jian Bioorganic and Medicinal Chemistry Letters, 2009 , vol. 19, # 15 p. 4292 - 4295
  • Route2
    • null|null
      3282-30-2
    • In-stock
      Thiosemicarbazide|CS-0008325
      79-19-6
    • ~%
    • In-stock
      5-(tert-Butyl)-1,3,4-thiadiazol-2-amine|CS-W010909
      39222-73-6

    References

    • Matti et al. Bulletin de la Societe Chimique de France, 1959 , p. 477

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302+H332
Precautionary Statements : P261-P264-P270-P271-P304+P340-P330-P501

Quality Control

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Computational Chemistry Data

  • TPSA   51.8
  • LogP   1.4178
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   0

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