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CS-W001157 4
Total: USD 88.00

5-Bromo-2-(bromomethyl)pyrimidine

  • CAS No. 1193116-74-3

  • Cat. No. CS-W019663
  • Purity≥96%
  • MDL No.MFCD16606298

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

5-Bromo-2-(bromomethyl)pyrimidine|CS-W019663

Structure of 1193116-74-3

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General Information

  • CAS No. 1193116-74-3
  • Cat. No. CS-W019663
  • Purity ≥96%
  • MDL No. MFCD16606298
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₄Br₂N₂
  • Molecular Weight None
  • Synonym(s) None
  • SMILES BrC1=CN=C(CBr)N=C1

Description

5-Bromo-2-(bromomethyl)pyrimidine features a bromomethyl group at the 2-position and a bromine atom at the 5-position of the pyrimidine ring, enabling dual electrophilic reactivity. This bifunctional scaffold facilitates efficient coupling in nucleophilic substitution reactions, particularly in the synthesis of heterocyclic compounds and pharmaceutical intermediates under standard conditions.

Application

5-Bromo-2-(bromomethyl)pyrimidine serves as a versatile di-functional building block in synthetic organic chemistry, enabling sequential functionalization at both the pyrimidine C5 and C2 positions. The bromomethyl group facilitates nucleophilic substitution reactions, while the C5-bromo substituent supports palladium-catalyzed cross-coupling processes. Its bench-stable nature and compatibility with standard protecting group strategies make it a practical reagent for constructing heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.

Safety Information

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GHS Pictogram :
GHS No : GHS05,GHS07
Signal Word : Danger
UN#: 3261
Class : 8
Packing Group : Ⅱ
Hazard Statements : H302-H314
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501

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Computational Chemistry Data

  • TPSA   25.78
  • LogP   2.134
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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