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CS-W001157 4
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6-Amino-3-bromo-2-methylbenzoic acid

  • CAS No. 124341-06-6

  • Cat. No. CS-0146987
  • Purity≥98%
  • MDL No.None

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

6-Amino-3-bromo-2-methylbenzoic acid|CS-0146987

Structure of 124341-06-6

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General Information

  • CAS No. 124341-06-6
  • Cat. No. CS-0146987
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₈BrNO₂
  • Molecular Weight 230.06
  • Synonym(s) Benzoic acid, 6-amino-3-bromo-2-methyl-
  • SMILES O=C(O)C1=C(N)C=CC(Br)=C1C

Description

6-Amino-3-bromo-2-methylbenzoic acid features a strategically positioned amino group enabling direct functionalization, while the bromo and methyl substituents enhance regioselectivity in cross-coupling reactions. This electron-rich scaffold supports efficient derivatization under standard conditions.

Application

6-Amino-3-bromo-2-methylbenzoic acid serves as a versatile building block for the synthesis of functionalized aromatic scaffolds. The molecule enables direct derivatization at the amino and carboxylic acid groups, while the bromo and methyl substituents support palladium-catalyzed cross-coupling reactions and regioselective electrophilic substitutions. Its bench-stable nature and compatibility with standard purification protocols make it well-suited for medicinal chemistry campaigns and process development.

Synthesis

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    • In-stock
      6-Amino-3-bromo-2-methylbenzoic acid|CS-0146987
      124341-06-6

    References

    • Journal of Medicinal Chemistry, , vol. 33, # 2 p. 814 - 819
  • Route2

    References

    • WO2013/177349 A2, ;

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

Quality Control

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Computational Chemistry Data

  • TPSA   63.32
  • LogP   2.03792
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   1

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