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CS-W001157 4
Total: USD 88.00

2-Methylimidazo[1,2-a]pyridin-6-amine

  • CAS No. 860258-05-5

  • Cat. No. CS-0035648
  • Purity≥97%
  • MDL No.MFCD09991758

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

2-Methylimidazo[1,2-a]pyridin-6-amine|CS-0035648

Structure of 860258-05-5

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General Information

  • CAS No. 860258-05-5
  • Cat. No. CS-0035648
  • Purity ≥97%
  • MDL No. MFCD09991758
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₉N₃
  • Molecular Weight 147.18
  • Synonym(s) IMidazo[1,2-a]pyridin-6-aMine, 2-Methyl-
  • SMILES CC1=CN2C=C(C=CC2=N1)N

Description

2-Methylimidazo[1,2-a]pyridin-6-amine delivers a rigid, electron-rich heterocyclic scaffold ideal for medicinal chemistry applications. This bench-stable core integrates seamlessly into kinase inhibitors and targeted therapeutics, offering enhanced binding affinity through complementary π-stacking and hydrogen bonding interactions.

Application

2-Methylimidazo[1,2-a]pyridin-6-amine serves as a versatile heterocyclic building block for medicinal chemistry and catalyst development. Its fused imidazo[1,2-a]pyridine core provides robust scaffold stability and favorable electronic properties, enabling efficient coupling reactions and metal-catalyzed transformations. The 6-amino group facilitates derivatization via amide formation, alkylation, or electrophilic substitution, while the methyl substituent enhances metabolic stability and modulates solubility. This compound exhibits excellent bench stability and compatibility with standard purification protocols, making it well-suited for high-throughput synthesis and API intermediate construction.

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   43.32
  • LogP   1.22492
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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