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CS-W001157 4
Total: USD 88.00

2-Chloro-1,3,4-thiadiazole

  • CAS No. 52819-57-5

  • Cat. No. CS-0072002
  • Purity≥95%
  • MDL No.MFCD17170010

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

2-Chloro-1,3,4-thiadiazole|CS-0072002

Structure of 52819-57-5

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General Information

  • CAS No. 52819-57-5
  • Cat. No. CS-0072002
  • Purity ≥95%
  • MDL No. MFCD17170010
  • Storage -20°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂HClN₂S
  • Molecular Weight None
  • Synonym(s) 1,3,4-Thiadiazole,2-chloro
  • SMILES ClC1=NN=CS1

Description

2-Chloro-1,3,4-thiadiazole is a heterocyclic compound featuring a chlorine atom at the 2-position, conferring enhanced electrophilicity and reactivity. This electron-deficient scaffold integrates readily into synthetic pathways requiring polarizable ring systems. The molecule exhibits bench-stable handling characteristics and serves as a key building block in medicinal chemistry and agrochemical development.

Application

2-Chloro-1,3,4-thiadiazole serves as a versatile electrophilic building block in heterocyclic synthesis, enabling efficient functionalization at the 2-position via nucleophilic substitution. Its stability under standard reaction conditions and compatibility with diverse nucleophiles facilitate access to substituted thiadiazoles used in medicinal chemistry and agrochemical scaffolds. The molecule functions as a key intermediate in the construction of bioactive heterocycles and exhibits favorable handling properties for routine bench-scale applications.

Synthesis

  • Route1

    References

    • Goerdeler et al. Chemische Berichte, 1956 , vol. 89, p. 1534,1540

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-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   25.78
  • LogP   1.1915
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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