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CS-W001157 4
Total: USD 88.00

3-Chloro-1H-pyrazol-4-amine

  • CAS No. 103286-54-0

  • Cat. No. CS-W007071
  • Purity≥95%
  • MDL No.MFCD23701740

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

3-Chloro-1H-pyrazol-4-amine|CS-W007071

Structure of 103286-54-0

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General Information

  • CAS No. 103286-54-0
  • Cat. No. CS-W007071
  • Purity ≥95%
  • MDL No. MFCD23701740
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃H₄ClN₃
  • Molecular Weight None
  • Synonym(s) 5-chloro-1H-pyrazol-4-amine
  • SMILES NC1=CNN=C1Cl

Description

3-Chloro-1H-pyrazol-4-amine features a chlorinated pyrazole core with a primary amine at the 4-position, enabling direct incorporation into diverse heterocyclic scaffolds. This bench-stable, moisture-tolerant building block facilitates efficient access to bioactive compounds through coupling reactions and nucleophilic substitution processes.

Application

3-Chloro-1H-pyrazol-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrazole-based heterocycles. Its chloro and amino groups offer orthogonal reactivity for C–H functionalization, Suzuki-Miyaura coupling, or amide formation. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns and API intermediate development.

Synthesis

  • Route1

    References

    • CELLZOME LIMITED; RAMSDEN, Nigel; HARRISON, Richard John; OXENFORD, Sally; BELL, Kathryn; PITON, Nelly; DAGOSTIN, Claudio; BOUSSARD, Cyrille; RATCLIFFE, Andrew Patent: WO2011/48082 A1, 2011 ; Location in patent: Page/Page column 115 ; WO 2011/048082 A1

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   54.7
  • LogP   0.6453
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   0

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