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CS-W001157 4
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(3-Bromo-5-chloropyridin-2-yl)methanol

  • CAS No. 1227599-26-9

  • Cat. No. CS-0042009
  • Purity≥98%
  • MDL No.MFCD16606988

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

(3-Bromo-5-chloropyridin-2-yl)methanol|CS-0042009

Structure of 1227599-26-9

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General Information

  • CAS No. 1227599-26-9
  • Cat. No. CS-0042009
  • Purity ≥98%
  • MDL No. MFCD16606988
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅BrClNO
  • Molecular Weight 222.47
  • Synonym(s) None
  • SMILES OCC1=NC=C(Cl)C=C1Br

Description

(3-Bromo-5-chloropyridin-2-yl)methanol features a pyridine core bearing bromo and chloro substituents at adjacent positions, enabling selective functionalization. The pendant hydroxymethyl group provides a handle for derivatization, facilitating incorporation into bioactive scaffolds. This bench-stable reagent combines high reactivity with predictable regiochemistry in cross-coupling and nucleophilic substitution processes.

Application

(3-Bromo-5-chloropyridin-2-yl)methanol serves as a versatile building block for late-stage functionalization in medicinal chemistry and agrochemical synthesis. Its dual halogenation pattern enables selective cross-coupling reactions, while the benzylic alcohol functionality facilitates derivatization via oxidation, protection, or substitution. The compound exhibits excellent bench stability and compatibility with standard Pd-catalyzed transformations, making it ideal for constructing complex heterocyclic scaffolds under mild conditions.

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   33.12
  • LogP   1.9898
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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