28022-22-2

Basic information

• Product Name: Benzene, (2-azido-2-propenyl)-
• CAS NO: 28022-22-2
• Molecular Formula: C9H9N3
• Molecular Weight: 159.191
• Mol File: 28022-22-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, (2-azido-2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (2-azido-2-propenyl)-(28022-22-2)
• EPA Substance Registry System: Benzene, (2-azido-2-propenyl)-(28022-22-2)

Safety Data

• Hazardous Substances Data: 28022-22-2(Hazardous Substances Data)

Upstream product

• 10147-11-2 propargyl benzene 
• 300-57-2 allylbenzene 
• 16484-04-1 2-Azido-1-iodo-3-phenylpropan 

Downstream Products

• 18709-44-9 C₉H₉N 
• 135608-75-2 benzyl carbamate 
• 49656-77-1 4-benzyl-2H-oxazol-5-one 
• 49656-73-7 4-benzyl-5-methoxy-5-trifluoromethyl-2,5-dihydro-oxazole 

Relevant articles and documents

Electrocatalytic Synthesis of gem -Bisarylthio Enamines and α-Phenylthio Ketones via a Radical Process under Mild Conditions

The novel method for the synthesis of gem -bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte at ro

Synthesis of β-Difluoroalkyl Azides via Elusive 1,2-Azide Migration

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Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines

An electron-withdrawing-group-generable radical-induced enamination of vinyl azides is reported, which results in a variety of β-functionalized N-unprotected enamines in a stereoselective manner. A plausible mechanism involving an unusual 1,3-H transfer of in situ generated iminyl radical intermediate was proposed on the basis of experimental results and DFT calculations.