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CS-W001157 4
Total: USD 88.00

7-Bromo-3-isoquinolinamine

  • CAS No. 1192815-02-3

  • Cat. No. CS-W008861
  • Purity≥95%
  • MDL No.MFCD11040207

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

7-Bromo-3-isoquinolinamine|CS-W008861

Structure of 1192815-02-3

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General Information

  • CAS No. 1192815-02-3
  • Cat. No. CS-W008861
  • Purity ≥95%
  • MDL No. MFCD11040207
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₇BrN₂
  • Molecular Weight 223.07
  • Synonym(s) 7-Bromoisoquinolin-3-amine; 7-Bromoisoquinolin-3-amine, 3-Amino-7-bromo-2-azanaphthalene
  • SMILES NC1=CC2=C(C=N1)C=C(Br)C=C2

Description

7-Bromo-3-isoquinolinamine features a bromine substituent at the 7-position and a primary amine at the 3-position of the isoquinoline core. This electron-deficient scaffold integrates readily into cross-coupling reactions, enabling direct access to functionalized heterocycles under standard conditions. The pendant amine facilitates downstream derivatization and serves as a handle for conjugation or metal coordination.

Application

7-Bromo-3-isoquinolinamine serves as a versatile building block for the synthesis of isoquinoline-based pharmaceuticals and functional materials. The bromo group enables palladium-catalyzed cross-coupling reactions, while the primary amine facilitates derivatization and salt formation. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis in medicinal chemistry and process development workflows.

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   38.91
  • LogP   2.5795
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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