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CS-W001157 4
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6-Chloro-1-methyl-1H-indazol-3-amine

  • CAS No. 1031927-22-6

  • Cat. No. CS-0440071
  • Purity≥98%
  • MDL No.None

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

6-Chloro-1-methyl-1H-indazol-3-amine|CS-0440071

Structure of 1031927-22-6

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General Information

  • CAS No. 1031927-22-6
  • Cat. No. CS-0440071
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₈ClN₃
  • Molecular Weight 181.62
  • Synonym(s) 6-chloro-1-methylindazol-3-amine
  • SMILES ClC=1C=CC=2C(=NN(C2C1)C)N

Description

6-Chloro-1-methyl-1H-indazol-3-amine features a chlorinated indazoline core with a methylated nitrogen and primary amine functionality. This electron-deficient heterocycle integrates readily into medicinal chemistry scaffolds, offering enhanced metabolic stability and tunable polarity for target engagement in kinase inhibition and CNS drug discovery.

Application

6-Chloro-1-methyl-1H-indazol-3-amine serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The chloro group at the 6-position offers high reactivity in Suzuki, Negishi, and Buchwald–Hartwig couplings, while the 3-amino and 1-methyl substituents provide orthogonal handles for further derivatization. Bench-stable and readily purified by chromatography or recrystallization, it functions reliably in API scaffold development and fragment-based drug discovery 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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   43.84
  • LogP   1.8089
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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