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CS-W001157 4
Total: USD 88.00

6-Bromo-7-methylpyrazolo[1,5-a]pyridine

  • CAS No. 1427382-24-8

  • Cat. No. CS-0160524
  • Purity≥98%
  • MDL No.MFCD23710616

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

6-Bromo-7-methylpyrazolo[1,5-a]pyridine|CS-0160524

Structure of 1427382-24-8

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General Information

  • CAS No. 1427382-24-8
  • Cat. No. CS-0160524
  • Purity ≥98%
  • MDL No. MFCD23710616
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇BrN₂
  • Molecular Weight 211.06
  • Synonym(s) 6-bromo-7-methyl-pyrazole [1,5-A]pyridine
  • SMILES CC1=C(Br)C=CC2=CC=NN12

Description

6-Bromo-7-methylpyrazolo[1,5-a]pyridine features a fused heterocyclic core with bromine and methyl substituents at distinct positions, enabling selective functionalization. The electron-deficient pyrazolopyridine scaffold supports efficient cross-coupling reactions under standard conditions, while the steric profile of the 7-methyl group enhances regioselectivity in palladium-catalyzed transformations. This bench-stable compound serves as a key building block for bioactive molecule synthesis.

Application

6-Bromo-7-methylpyrazolo[1,5-a]pyridine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo functionality. The methyl group at the 7-position enhances regiochemical control and improves solubility in organic media. This compound functions effectively in Suzuki-Miyaura and Stille couplings, facilitating efficient access to substituted pyrazolopyridine scaffolds relevant to medicinal chemistry and materials science.

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-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   17.3
  • LogP   2.40522
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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