129995-39-7

Basic information

• Product Name: 2-(tetrahydrofuran-2-yl)-2H-benzo[d][1,2,3]triazole
• CAS NO: 129995-39-7
• Molecular Weight: 189.217
• Mol File: 129995-39-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(tetrahydrofuran-2-yl)-2H-benzo[d][1,2,3]triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(tetrahydrofuran-2-yl)-2H-benzo[d][1,2,3]triazole(129995-39-7)
• EPA Substance Registry System: 2-(tetrahydrofuran-2-yl)-2H-benzo[d][1,2,3]triazole(129995-39-7)

Safety Data

• Hazardous Substances Data: 129995-39-7(Hazardous Substances Data)

Upstream product

• 109-99-9 tetrahydrofuran 
• 95-14-7 1,2,3-Benzotriazole 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 43183-36-4 1-(trimethylsilyl)-1H-benzotriazole 
• 1191-99-7 2,3-dihydro-2H-furan 
• 28539-02-8 1-Hydroxymethyl-1H-benzotriazole 
• 6872-06-6 2-methyl indoline 
• 50-00-0 formaldehyd 
• 496-15-1 1-indoline 

Relevant articles and documents

Ruthenium-Catalyzed C-H Bond Activation Approach to Azolyl Aminals and Hemiaminal Ethers, Mechanistic Evaluations, and Isomer Interconversion

C(sp3)-N bond-forming reactions between benzotriazole and 5,6-dimethylbenzotriazole with N-methylpyrrolidinone, tetrahydrofuran, tetrahydropyran, diethyl ether, 1,4-dioxane, and isochroman have been conducted using RuCl3·3H2/su

Synthesis of novel 1,2,5,6-tetrahydro-4H-pyrrolo[3,2,1-ij]quinolines via benzotriazole methodology

Pyrroloquinolines have been synthesized reacting 1-(benzotriazol-1(2)-ylmethyl)indolines with unactivated and electron-rich alkenes in the presence of p-toluenesulfonic acid catalyst. Mixtures of the expected diastereomers were obtained and some of them s

Decatungstate-Mediated C(sp3)–H Heteroarylation via Radical-Polar Crossover in Batch and Flow

Photocatalytic hydrogen atom transfer is a very powerful strategy for the regioselective C(sp3)–H functionalization of organic molecules. Herein, we report on the unprecedented combination of decatungstate hydrogen atom transfer photocatalysis with the oxidative radical–polar crossover concept to access the direct net-oxidative C(sp3)–H heteroarylation. The present methodology demonstrates a high functional group tolerance (40 examples) and is scalable when using continuous-flow reactor technology. The developed protocol is also amenable to the late-stage functionalization of biologically relevant molecules such as stanozolol, (?)-ambroxide, podophyllotoxin, and dideoxyribose.