75867-47-9

Basic information

• Product Name: Silane, trimethyl[(2-nitrophenyl)ethynyl]-
• CAS NO: 75867-47-9
• Molecular Formula: C11H13NO2Si
• Molecular Weight: 219.315
• Mol File: 75867-47-9.mol
• Article Data: 34

Chemical Properties

• CAS DataBase Reference: Silane, trimethyl[(2-nitrophenyl)ethynyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, trimethyl[(2-nitrophenyl)ethynyl]-(75867-47-9)
• EPA Substance Registry System: Silane, trimethyl[(2-nitrophenyl)ethynyl]-(75867-47-9)

Safety Data

• Hazardous Substances Data: 75867-47-9(Hazardous Substances Data)

Upstream product

• 577-19-5 2-nitrophenyl bromide 
• 1066-54-2 trimethylsilylacetylene 
• 609-73-4 o-nitroiodobenzene 
• 109-89-7 diethylamine 
• 121-44-8 triethylamine 
• 7087-68-5 N-ethyl-N,N-diisopropylamine 

Downstream Products

• 25410-92-8 2-[2-(2-nitrophenyl)-2-oxoethylidene]-1,2-dihydroindole-3-one 
• 91-56-5 indole-2,3-dione 
• 1158998-66-3 1-benzyl-4-(2-nitrophenyl)-1H-1,2,3-triazole 
• 113783-27-0 1-(2-iodoethynyl)-2-nitrobenzene 
• 17961-94-3 2-[2'-trimethylsilylethyl]aniline 
• 120-72-9 indole 
• 116548-00-6 N-<2-(Trimethylsilylethynyl)phenyl>methanesulfonamide 
• 91873-11-9 2-aminophenylacetaldehyde diethyl acetal 
• 133253-56-2 2,2'-dinitrobenzil 

Relevant articles and documents

Electrochemically Enabled Selenium Catalytic Synthesis of 2,1-Benzoxazoles fromo-Nitrophenylacetylenes

The study reported an electrochemically mediated method for the preparation of 2,1-benzoxazoles fromo-nitrophenylacetylenes. Different from the traditional electrochemical reduction of nitro to nitroso, the nitro group directly underwent a cyclization rea

Oxidative Approach Enables Efficient Access to Cyclic Azobenzenes

Azobenzenes are versatile photoswitches that have found widespread use in a variety of fields, ranging from photopharmacology to the material sciences. In addition to regular azobenzenes, the cyclic diazocines have recently emerged. Although diazocines have fascinating conformational and photophysical properties, their use has been limited by their synthetic accessibility. Herein, we present a general, high-yielding protocol that relies on the oxidative cyclization of dianilines. In combination with a modular substrate synthesis, it allows for rapid access to diversely functionalized diazocines on gram scales. Our work systematically explores substituent effects on the photoisomerization and thermal relaxation of diazocines. It will enable their incorporation into a wide variety of functional molecules, unlocking the full potential of these emerging photoswitches. The method can be applied to the synthesis of a new cyclic azobenzene with a nine-membered central ring and distinct properties.

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

A heterocyclic compound and an organic light-emitting device including the heterocyclic compound, the heterocyclic compound being represented by Formula 1: