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CS-W001157 4
Total: USD 88.00

6-Chloro-2-methyl-2H-indazol-5-amine

  • CAS No. 1893125-36-4

  • Cat. No. CS-0375281
  • Purity≥98%
  • MDL No.None

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

6-Chloro-2-methyl-2H-indazol-5-amine|CS-0375281

Structure of 1893125-36-4

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General Information

  • CAS No. 1893125-36-4
  • Cat. No. CS-0375281
  • 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) Ensitrelvir Intermediate
  • SMILES NC1=CC2=CN(C)N=C2C=C1Cl

Description

6-Chloro-2-methyl-2H-indazol-5-amine features a chlorinated indazole core with a methyl group at the 2-position and a primary amine at the 5-position. This electron-deficient scaffold enables direct coupling in cross-coupling reactions, serving as a key building block for bioactive heterocycles in medicinal chemistry and agrochemical development.

Application

6-Chloro-2-methyl-2H-indazol-5-amine serves as a versatile building block for medicinal chemistry and agrochemical synthesis, enabling efficient construction of indazole-based scaffolds. The chloro group facilitates palladium-catalyzed cross-coupling reactions, while the primary amine supports derivatization via acylation, alkylation, or reductive amination. Bench-stable and readily purified by chromatography, it functions reliably in standard synthetic workflows requiring functional group tolerance and predictable reactivity.

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
Precautionary Statements : P264-P280-P302+P352-P362

Quality Control

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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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