172265-11-1

Basic information

• Product Name: 1-(ethoxy(p-tolyl)methyl)-1H-benzotriazole
• Synonyms: 1-(ethoxy(p-tolyl)methyl)-1H-benzotriazole
• CAS NO: 172265-11-1
• Molecular Weight: 267.33
• Mol File: 172265-11-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(ethoxy(p-tolyl)methyl)-1H-benzotriazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(ethoxy(p-tolyl)methyl)-1H-benzotriazole(172265-11-1)
• EPA Substance Registry System: 1-(ethoxy(p-tolyl)methyl)-1H-benzotriazole(172265-11-1)

Safety Data

• Hazardous Substances Data: 172265-11-1(Hazardous Substances Data)

Upstream product

• 95-14-7 1,2,3-Benzotriazole 
• 104-87-0 4-methyl-benzaldehyde 
• 122-51-0 orthoformic acid triethyl ester 
• 64-17-5 ethanol 

Downstream Products

• 1370291-57-8 potassium trifluoro(4-methylbenzoyl)borate 
• 130649-66-0 1-(4-Methylphenyl)-3-buten-1-one 
• 172265-06-4 2-phenyl-2-(phenylamino)-1-(p-tolyl)ethanone 
• 1027886-23-2 1-(1-Ethoxy-1-p-tolyl-but-3-enyl)-1H-benzotriazole 

Relevant articles and documents

Synthesis of Polymers Containing Potassium Acyltrifluoroborates (KATs) and Post-polymerization Ligation and Conjugation

We report the synthesis of monomers for atom-transfer radical polymerization (ATRP) and a reversible addition-fragmentation chain transfer (RAFT) agent bearing trifluoroborate iminiums (TIMs), which are quantitatively converted into potassium acyltrifluor

Benzotriazole-Mediated Conversions of Aromatic and Heteroaromatic Aldehydes to Functionalized Ketones

Aromatic and heteroaromatic aldehydes reacted with benzotriazole and triethyl orthoformate in THF to give the corresponding α-(benzotriazol-1-yl)aryl ethyl ethers 7 in good yield.The novel acyl anion precursors 7 underwent smooth lithiation at the methine group followed by trapping with alkyl halides, aldehydes, ketones, and imines to yield the expected substituted intermediates of type 9, which were hydrolyzed under mild conditions without isolation.Benzaldehyde, methyl-, chloro-, and methoxy-substituted benzaldehydes, 1-naphthalenecarboxaldehyde, 2- and 3-furaldehydes, 2- and 3-thiophenecarboxaldehydes, and 2-pyridinecarboxaldehyde were all transformed in this manner into a variety of aryl and heteroaryl ketones with alkyl (10), α-hydroxyalkyl (12 and 13), α-aminoalkyl (14) and acyl (15) substituents.