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CS-W001157 4
Total: USD 88.00

2-Amino-5-bromo-4-methylbenzoic acid

  • CAS No. 106976-24-3

  • Cat. No. CS-0145126
  • Purity≥98%
  • MDL No.MFCD12026295

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

2-Amino-5-bromo-4-methylbenzoic acid|CS-0145126

Structure of 106976-24-3

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General Information

  • CAS No. 106976-24-3
  • Cat. No. CS-0145126
  • Purity ≥98%
  • MDL No. MFCD12026295
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₈BrNO₂
  • Molecular Weight 230.06
  • Synonym(s) None
  • SMILES O=C(C1=CC(Br)=C(C=C1N)C)O

Description

This brominated benzoic acid derivative features a para-substituted amino group and a methyl moiety, enabling direct integration into diverse synthetic scaffolds. The carboxylic acid functionality supports facile derivatization under standard coupling conditions, while the electron-withdrawing bromine enhances reactivity in cross-coupling processes. Bench-stable and moisture-tolerant, this compound serves as a key intermediate in pharmaceutical and agrochemical synthesis.

Application

2-Amino-5-bromo-4-methylbenzoic acid serves as a versatile building block for the synthesis of heterocyclic scaffolds and bioactive molecules. Its well-defined functional group array—amino, bromo, methyl, and carboxylic acid—enables sequential transformations via Suzuki coupling, amidation, and electrophilic substitution. The compound exhibits good bench stability and facilitates straightforward purification, making it suitable for iterative medicinal chemistry campaigns and API intermediate 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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-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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