66571-35-5

Basic information

• Product Name: 1-(2,6-dimethyl-4-pyridinyl)-1H-1,2,3-benzotriazole
• Synonyms: 1-(2,6-dimethyl-4-pyridinyl)-1H-1,2,3-benzotriazole
• CAS NO: 66571-35-5
• Molecular Formula: C13H12N4
• Molecular Weight: 224.26118
• Mol File: 66571-35-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(2,6-dimethyl-4-pyridinyl)-1H-1,2,3-benzotriazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,6-dimethyl-4-pyridinyl)-1H-1,2,3-benzotriazole(66571-35-5)
• EPA Substance Registry System: 1-(2,6-dimethyl-4-pyridinyl)-1H-1,2,3-benzotriazole(66571-35-5)

Safety Data

• Hazardous Substances Data: 66571-35-5(Hazardous Substances Data)

Upstream product

• 3512-75-2 4-chloro-2,6-lutidine 
• 95-14-7 1,2,3-Benzotriazole 

Downstream Products

• 46382-84-7 1,3-dimethyl-5H-pyrido<4,3-b>indole 

Relevant articles and documents

Synthesis and DNA binding properties of γ-carbolinium derivatives and benzologues

The 5H-pyrido[4,3-b]indole, 11H-indolo[3,2-c]quinoline, 5H-benzo[f]pyrido[4,3-b]indole, and 13H-benz[5,6]indolo[3,2-c]quinoline heteroaromatic nuclei have been synthesized by the Graebe-Ullmann method by classical heating or under microwave irradiation. These tri-, tetra-, and pentacyclic compounds were transformed into the corresponding cationic derivatives by N-alkylation, and the DNA-binding properties of the resulting cationic systems were examined using UV-vis spectroscopy, viscometric determinations, and molecular modeling techniques. The tetracyclic cations were transformed into bis-salts by means of a diethyl bispiperidine rigid chain and a more flexible polyamide linker, but the low solubility of these bis-salts made the study of their bisintercalating properties difficult.