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CS-W001157 4
Total: USD 88.00

1-Ethylpyrazole-4-sulfonyl chloride

  • CAS No. 957514-21-5

  • Cat. No. CS-0061518
  • Purity≥95%
  • MDL No.None

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

1-Ethylpyrazole-4-sulfonyl chloride|CS-0061518

Structure of 957514-21-5

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General Information

  • CAS No. 957514-21-5
  • Cat. No. CS-0061518
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₇ClN₂O₂S
  • Molecular Weight 194.64
  • Synonym(s) None
  • SMILES CCN1C=C(C=N1)S(=O)(=O)Cl

Description

1-Ethyl-1H-pyrazole-4-sulfonyl chloride features a reactive sulfonyl chloride group tethered to a pyrazole scaffold, enabling efficient coupling in heterocyclic synthesis. The ethyl substituent enhances solubility and modulates electronic properties, while the bench-stable nature facilitates handling under standard conditions. This reagent integrates readily into pharmaceutical and agrochemical development workflows.

Application

1-Ethyl-1H-pyrazole-4-sulfonyl chloride serves as a versatile sulfonyl chloride building block for the synthesis of sulfonamide derivatives. Its pyrazole scaffold provides structural rigidity and enhanced metabolic stability, while the reactive sulfonyl chloride group enables efficient coupling with amines under mild conditions. The ethyl substituent enhances solubility and facilitates purification. This reagent is bench-stable, compatible with common functional groups, and widely used in medicinal chemistry for constructing bioactive heterocyclic scaffolds.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3265
Class : 8
Packing Group : Ⅲ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   51.96
  • LogP   0.8305
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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