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CS-W001157 4
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2-(5-Bromopyrimidin-2-yl)acetic acid

  • CAS No. 1134327-93-7

  • Cat. No. CS-0018844
  • Purity≥95%
  • MDL No.MFCD09909705

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

2-(5-Bromopyrimidin-2-yl)acetic acid|CS-0018844

Structure of 1134327-93-7

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General Information

  • CAS No. 1134327-93-7
  • Cat. No. CS-0018844
  • Purity ≥95%
  • MDL No. MFCD09909705
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅BrN₂O₂
  • Molecular Weight 217.02
  • Synonym(s) (5-Bromopyrimidin-2-yl)acetic acid
  • SMILES O=C(O)CC1=NC=C(Br)C=N1

Description

This bromopyrimidine-acetic acid derivative features a reactive bromine at the 5-position of a pyrimidine ring, enabling efficient cross-coupling transformations. The carboxylic acid group provides a versatile handle for conjugation and derivatization under standard conditions. Designed for synthetic versatility in medicinal chemistry and materials science applications.

Application

2-(5-Bromopyrimidin-2-yl)acetic acid serves as a versatile building block for the synthesis of pyrimidine-based pharmaceuticals and agrochemicals. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates derivatization via amide or ester formation. Its bench-stable nature and compatibility with common protecting group strategies make it a practical reagent for 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   63.08
  • LogP   0.8662
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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