1423122-45-5

Basic information

• Product Name: p-tolyl(4-bromo-2,6-dimethoxy-5-pyrimidinyl)methanol
• Synonyms: p-tolyl(4-bromo-2,6-dimethoxy-5-pyrimidinyl)methanol
• CAS NO: 1423122-45-5
• Molecular Weight: 339.189
• Mol File: 1423122-45-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-tolyl(4-bromo-2,6-dimethoxy-5-pyrimidinyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: p-tolyl(4-bromo-2,6-dimethoxy-5-pyrimidinyl)methanol(1423122-45-5)
• EPA Substance Registry System: p-tolyl(4-bromo-2,6-dimethoxy-5-pyrimidinyl)methanol(1423122-45-5)

Safety Data

• Hazardous Substances Data: 1423122-45-5(Hazardous Substances Data)

Upstream product

• 56686-16-9 5-bromo-2,4-dimethoxypyrimidine 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 1423122-47-7 p-tolyl(4-(trimethylsilylethynyl)-2,6-dimethoxy-5-pyrimidineyl)methanone 
• 1423122-48-8 C₁₆H₁₄N₂O₃ 
• 1423122-46-6 p-tolyl(4-bromo-2,6-dimethoxy-5-pyrimidineyl)methanone 

Relevant articles and documents

Synthesis of azahomosteroid ring system through intramolecular [4+2] cycloaddition of in situ generated azaisobenzofuran intermediates

Azahomosteroid ring systems were synthesized through two-component coupling of γ,δ-unsaturated Fischer carbene complexes with o-alkynylheteroaryl carbonyl derivatives. The reaction occurs through the formation of azaisobenzofuran as transient intermediate; the latter undergoes a subsequent Diels-Alder cycloaddition reaction with in-built dienophile with high regio- and stereoselectivity. Copyright