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CS-W001157 4
Total: USD 88.00

(5-Methyl-1,3,4-thiadiazol-2-yl)methanol

  • CAS No. 869108-51-0

  • Cat. No. CS-0187970
  • Purity≥97%
  • MDL No.None

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

(5-Methyl-1,3,4-thiadiazol-2-yl)methanol|CS-0187970

Structure of 869108-51-0

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General Information

  • CAS No. 869108-51-0
  • Cat. No. CS-0187970
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₆N₂OS
  • Molecular Weight 130.17
  • Synonym(s) None
  • SMILES CC1=NN=C(CO)S1

Description

(5-Methyl-1,3,4-thiadiazol-2-yl)methanol features a methyl-substituted thiadiazole ring linked to a primary alcohol group, delivering enhanced solubility and reactivity. This scaffold integrates readily into heterocyclic synthesis, serving as a versatile synthon for medicinal chemistry and materials science applications.

Application

(5-Methyl-1,3,4-thiadiazol-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through its reactive methylene group. The molecule exhibits bench stability and tolerates common functional groups, facilitating straightforward incorporation into diverse scaffolds via nucleophilic substitution or coupling reactions. Its well-defined reactivity profile supports efficient synthesis of potential drug candidates and functionalized intermediates in standard organic workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330-P501

Quality Control

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Computational Chemistry Data

  • TPSA   46.01
  • LogP   0.33882
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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