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CS-W001157 4
Total: USD 88.00

5-Bromo-4-methoxy-2-methylpyridine

  • CAS No. 886372-61-8

  • Cat. No. CS-0146051
  • Purity≥98%
  • MDL No.MFCD07374958

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

5-Bromo-4-methoxy-2-methylpyridine|CS-0146051

Structure of 886372-61-8

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General Information

  • CAS No. 886372-61-8
  • Cat. No. CS-0146051
  • Purity ≥98%
  • MDL No. MFCD07374958
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₈BrNO
  • Molecular Weight 202.05
  • Synonym(s) 5-BROMO-4-METHOXY-2-METHYL-PYRIDINE
  • SMILES CC1=NC=C(Br)C(OC)=C1

Description

5-Bromo-4-methoxy-2-methylpyridine features a pyridine core functionalized with bromo, methoxy, and methyl groups at strategic positions, enabling selective cross-coupling reactions. The electron-deficient aromatic ring pairs with the ortho-directed methyl group to facilitate regioselective transformations. This bench-stable building block integrates efficiently into pharmaceutical intermediates and agrochemical scaffolds.

Application

5-Bromo-4-methoxy-2-methylpyridine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine substituent. The methoxy and methyl groups provide orthogonal functional handles for further derivatization, while the pyridine core offers favorable electronic properties and stability under standard reaction conditions. Its bench-stable nature and compatibility with common synthetic protocols make it well-suited for modular scaffold construction in API 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 : 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   22.12
  • LogP   2.16112
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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