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CS-W001157 4
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7-Bromoisoquinolin-1-amine

  • CAS No. 215453-53-5

  • Cat. No. CS-W005231
  • Purity≥96%
  • MDL No.MFCD07374397

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

7-Bromoisoquinolin-1-amine|CS-W005231

Structure of 215453-53-5

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General Information

  • CAS No. 215453-53-5
  • Cat. No. CS-W005231
  • Purity ≥96%
  • MDL No. MFCD07374397
  • 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-Bromo-1-isoquinolinamine
  • SMILES NC1=NC=CC2=C1C=C(Br)C=C2

Description

7-Bromoisoquinolin-1-amine delivers a brominated isoquinoline scaffold with a primary amine at the 1-position, enabling direct functionalization in cross-coupling and medicinal chemistry applications. The electron-deficient ring system enhances reactivity in palladium-catalyzed transformations, while the pendant amine offers versatility for derivatization. This bench-stable, moisture-tolerant heterocycle serves as a key building block for kinase inhibitors and bioactive alkaloid analogs.

Application

7-Bromoisoquinolin-1-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C7 position via palladium-catalyzed cross-coupling reactions. The amine group facilitates conjugation and derivatization, while the bromide offers orthogonal reactivity for late-stage modifications. Its stability under standard synthetic conditions and compatibility with diverse transformations make it ideal for constructing complex heterocyclic scaffolds in API development.

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

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