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CS-W001157 4
Total: USD 88.00

3-Bromo-1-methyl-1H-pyrazol-5-amine

  • CAS No. 1357471-14-7

  • Cat. No. CS-W021850
  • Purity≥97%
  • MDL No.MFCD18800831

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

3-Bromo-1-methyl-1H-pyrazol-5-amine|CS-W021850

Structure of 1357471-14-7

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General Information

  • CAS No. 1357471-14-7
  • Cat. No. CS-W021850
  • Purity ≥97%
  • MDL No. MFCD18800831
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₆BrN₃
  • Molecular Weight 176.02
  • Synonym(s) 5-Amino-3-bromo-1-methylpyrazole
  • SMILES CN1N=C(Br)C=C1N

Description

3-Bromo-1-methyl-1H-pyrazol-5-amine features a brominated pyrazole core with a methylated nitrogen and a primary amine at the 5-position, enabling direct coupling in cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the methyl group enhances stability and solubility. This scaffold serves as a key intermediate in medicinal chemistry for targeted compound libraries.

Application

3-Bromo-1-methyl-1H-pyrazol-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyrazole scaffolds via palladium-catalyzed cross-coupling reactions. The bromine moiety facilitates reliable C–X bond formation under standard conditions, while the N-methylated pyrazole core offers enhanced metabolic stability and favorable solubility profiles. Its bench-stable nature and compatibility with diverse functional groups make it ideal for modular synthesis of bioactive compounds and API intermediates.

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

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Computational Chemistry Data

  • TPSA   43.84
  • LogP   0.7648
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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