111098-80-7

Basic information

• Product Name: bis(benzotriazolo)(4-methylphenyl)methane
• Synonyms: bis(benzotriazolo)(4-methylphenyl)methane
• CAS NO: 111098-80-7
• Molecular Weight: 340.387
• Mol File: 111098-80-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: bis(benzotriazolo)(4-methylphenyl)methane(CAS DataBase Reference)
• NIST Chemistry Reference: bis(benzotriazolo)(4-methylphenyl)methane(111098-80-7)
• EPA Substance Registry System: bis(benzotriazolo)(4-methylphenyl)methane(111098-80-7)

Safety Data

• Hazardous Substances Data: 111098-80-7(Hazardous Substances Data)

Upstream product

• 15217-42-2 sodium benzotriazolate 
• 113700-15-5 1-(Bromo-p-tolyl-methyl)-pyridinium; bromide 
• 95-14-7 1,2,3-Benzotriazole 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 142087-16-9 1-(4-methylbenzyl)-1H-benzo[d][1,2,3]triazole 
• 2001-28-7 2-phenyl-1-p-tolyl-ethanone 
• 122-00-9 para-methylacetophenone 
• 111508-19-1 C₃₁H₃₂N₆OSi 
• 111508-18-0 C₃₀H₃₀N₆OSi 
• 111508-20-4 C₂₇H₃₂N₆OSi 
• 111508-17-9 bis(benzotriazol-1-yl)-(3-oxocyclohexyl)-p-tolylmethane 
• 111508-16-8 2,2-Bis-benzotriazol-1-yl-1-phenyl-2-p-tolyl-ethanone 
• 111508-12-4 C₂₆H₂₈N₆ 
• 111508-13-5 bis(benzotriazol-1-yl)(benzyl)-p-tolylmethane 
• 111508-10-2 C₂₄H₂₄N₆ 
• 111508-11-3 C₂₄H₂₄N₆ 
• 111508-15-7 1,1-Bis-benzotriazol-1-yl-1-p-tolyl-propan-2-one 
• 111508-09-9 C₂₃H₂₂N₆ 

Relevant articles and documents

Construction of 3-aryl-1,2,4-benzotriazines via unprecedented rearrangement of bis(benzotriazol-1-yl)methylarenes

3-Aryl-1,2,4-benzotriazines were formed unexpectedly by the treatment of 1,l-bis(benzotriazol-1-yl)methylarenes with allylsamarium bromide. A radical pathway was proposed involving steps, such as fragmentation, ring-opening, and cyclization.

N-(1-Haloalkyl)pyridinium Salts: Preparation and Use for New Syntheses of Other N-(1-Substituted-alkyl)pyridinium Salts, N,N'-(1-Alkylidene)bisamines, and N,N'-(1-Alkylidene)bisbenzazoles

N-(1-Haloalkyl)pyridinium halides, obtained from an aldehyde, a thionyl halide, and pyridine, react readily with nucleophiles to yield N-(1-substituted -alkyl)pyridinium salts.N-(1-Bromoalkyl)pyridinium bromides rect readily with a wide range of nucleophiles to replace either the halogen ( by 1 mol ) or both halogen and pyridinium ( 2 mol ).They are useful precursors for the preparation of bisbenzazoles and other aminals under neutral and mild conditions.