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CS-W001157 4
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2-Amino-5-bromobenzamide

  • CAS No. 16313-66-9

  • Cat. No. CS-W008987
  • Purity≥98%
  • MDL No.MFCD04037881

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

2-Amino-5-bromobenzamide|CS-W008987

Structure of 16313-66-9

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General Information

  • CAS No. 16313-66-9
  • Cat. No. CS-W008987
  • Purity ≥98%
  • MDL No. MFCD04037881
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₇BrN₂O
  • Molecular Weight 215.05
  • Synonym(s) 5-Bromoanthranilamide; 5-Methoxy-phthalicacid
  • SMILES O=C(N)C1=CC(Br)=CC=C1N

Description

2-Amino-5-bromobenzamide features a brominated aromatic ring paired with dual amine and amide functionalities, enabling direct incorporation into pharmaceutical scaffolds. The para-positioned bromine facilitates cross-coupling reactions, while the amino group offers a handle for derivatization under mild conditions. This compound exhibits robust stability and solubility in polar organic solvents, streamlining use in synthetic workflows.

Application

2-Amino-5-bromobenzamide serves as a versatile building block in medicinal chemistry, enabling direct incorporation into heterocyclic scaffolds via amidation, Suzuki-Miyaura coupling, or electrophilic substitution. The ortho-amino and bromo groups provide complementary reactivity for sequential functionalization, while the amide functionality enhances solubility and metabolic stability. Bench-stable and readily purified by recrystallization, it facilitates efficient synthesis of kinase inhibitors and other bioactive compounds.

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   69.11
  • LogP   1.1302
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   1

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