CAS 114969-66-3: 5-bromopyrimidine-4-carbonitrile

Description: 5-Bromopyrimidine-4-carbonitrile is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a bromine atom at the 5-position and a cyano group at the 4-position. This compound typically exhibits a pale yellow to light brown appearance and is soluble in polar organic solvents. The presence of the bromine atom introduces notable electrophilic properties, making it a useful intermediate in various chemical syntheses, particularly in the development of pharmaceuticals and agrochemicals. The cyano group contributes to its reactivity, allowing for further functionalization through nucleophilic addition or substitution reactions. Additionally, 5-bromopyrimidine-4-carbonitrile can participate in cross-coupling reactions, which are valuable in constructing complex molecular architectures. Its unique structural features and reactivity profile make it an important building block in organic synthesis and medicinal chemistry. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₅H₂BrN₃

InChI: InChI=1/C5H2BrN3/c6-4-2-8-3-9-5(4)1-7/h2-3H

Synonyms:

• 4-Pyrimidinecarbonitrile, 5-Bromo-

4-Pyrimidinecarbonitrile, 5-bromo-

CAS: 114969-66-3

• Formula: C₅H₂BrN₃
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 183.9935

5-Bromopyrimidine-4-carbonitrile

CAS: 114969-66-3

• Purity: 0.95
• Molecular weight: 184.00g/mol

5-Bromo-4-cyanopyrimidine

CAS: 114969-66-3

• Purity: 95.0%
• Color and Shape: Liquid, No data available.
• Molecular weight: 183.99600219726562

5-Bromo-4-Pyrimidinecarbonitrile

CAS: 114969-66-3

5-Bromo-4-pyrimidinecarbonitrile is an efficient and scalable process for the synthesis of trimethylsilyl cyanide. The reaction …

• Formula: C₅H₂BrN₃
• Purity: Min. 95%
• Molecular weight: 183.99 g/mol