1394809-62-1

Basic information

• Product Name: 3,6-bis(2-(trimethylsilyl)ethynyl)benzene-1,2-diamine
• Synonyms: 3,6-bis(2-(trimethylsilyl)ethynyl)benzene-1,2-diamine
• CAS NO: 1394809-62-1
• Molecular Weight: 300.551
• Mol File: 1394809-62-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 3,6-bis(2-(trimethylsilyl)ethynyl)benzene-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-bis(2-(trimethylsilyl)ethynyl)benzene-1,2-diamine(1394809-62-1)
• EPA Substance Registry System: 3,6-bis(2-(trimethylsilyl)ethynyl)benzene-1,2-diamine(1394809-62-1)

Safety Data

• Hazardous Substances Data: 1394809-62-1(Hazardous Substances Data)

Upstream product

• 480998-11-6 4,7-bis[(trimethylsilyl)ethynyl]benzo[c][1,2,5]thiadiazole 
• 69272-50-0 1,2-diamine-3,6-dibromobenzene 
• 1066-54-2 trimethylsilylacetylene 
• 15155-41-6 4,7-dibromobenzo[c][1,2,5]thiadiazole 
• 273-13-2 benzo[1,2,5]thiadiazole 
• 95-54-5 1,2-diamino-benzene 

Relevant articles and documents

D-π-A benzo[c][1,2,5]selenadiazole-based derivatives via an ethynyl bridge: Photophysical properties, solvatochromism and applications as fluorescent sensors

A series of novel D-π-A benzo[c][1,2,5]selenadiazole (BSe)-based derivatives 7a-i including electron-donating/electron-withdrawing groups were prepared by Pd-catalyzed Sonogashira-Hagihara reaction of 4,7- diethynylbenzoselenadiazole with various diiodo a

Highly sensitive conjugated polymer fluorescent sensors based on benzochalcogendiazole for nickel ions in real-time detection

Reports about fluorescent sensors for the highly sensitive and selective detection of Ni2+ are rare compared with Hg2+, Ag +, Cd2+, Pb2+, Cr3+, etc. Herein, we report the synthesis and appl

Synthesis, characterization and electrochemistry of polycyclic fused aromatic pyrroles and their conjugated polymers

Polycyclic fused aromatic pyrrole-based compounds, benzodipyrrole, naphthobipyrrole and their alkylated derivatives, were synthesized and studied electrochemically. Amongst these, naphthobipyrrole having a tetracyclic fused aromatic structure was electrochemically polymerized to give the homopolymer of naphthobipyrrole, poly(naphthobipyrrole), indicating good reactivity of α,α′-pyrrolic positions towards oxidative coupling. As a strategic approach towards the synthesis of copolymers, naphthobipyrrole was copolymerized with arylaldehyde to afford poly(arylmethylene naphthobipyrrole) by exploring the reactivity of β,β′-pyrrolic positions. Moreover, optical and electrochemical studies showed that the copolymer possessed a low optical bandgap and an elevated HOMO level. The scan rate dependent cyclic voltammetry studies of the copolymer film showed the formation of an electroactive material.