1034917-77-5

Basic information

• Product Name: (Z)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)stilbene
• CAS NO: 1034917-77-5
• Molecular Weight: 432.176
• Mol File: 1034917-77-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (Z)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)stilbene(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)stilbene(1034917-77-5)
• EPA Substance Registry System: (Z)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)stilbene(1034917-77-5)

Safety Data

• Hazardous Substances Data: 1034917-77-5(Hazardous Substances Data)

Usage

General Description

(Z)-4-(4-4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)stilbene is a chemical compound that consists of a stilbene backbone with two boron-containing groups attached. The compound is classified as a boron-containing stilbene derivative. (Z)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)stilbene has potential applications in materials science and organic electronics due to its unique structural features and properties. It may also be used as a building block for the synthesis of more complex organic molecules. Additionally, the boron-containing groups may confer specific reactivity and properties to the compound, making it useful in various chemical processes and reactions.

Upstream product

• 870004-04-9 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)styrene 
• 1257648-79-5 6-methyl-2-(4-vinylphenyl)-1,3,6,2-dioxazaborocane-4,8-dione 
• 2156-04-9 4-Vinylphenylboronic acid 
• 76-09-5 2,3-dimethyl-2,3-butane diol 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 23958-29-4 (Z)-4,4'-dibromostilbene 
• 1122-91-4 4-bromo-benzaldehyde 
• 51044-13-4 4-bromobenzyl triphenylphosphonium bromide 
• 1169942-85-1 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-3-yl-phenyl)-methyl triphenylphosphonium bromide 
• 128376-64-7 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde 
• 849681-64-7 (1,2-bis(4-(4,4,5,5-tetramethyl--1,3,2-dioxaborolan-2yl)phenyl)acetylene) 
• 195062-57-8 p-tolylboronic pinacol ester 
• 138500-85-3 4-bromomethylphenylboronic acid pinacol ester 
• 18869-30-2 (E)-4,4'-dibromostilbene 

Relevant articles and documents

A Twisted Nanographene Consisting of 96 Carbon Atoms

Herein we report synthesis, structure and properties of a new type of twisted nanographene, which contains an [8]circulene moiety in a polycyclic framework of 96 sp2 carbon atoms. The key steps in this synthesis are the Diels–Alder reaction of a macrocyclic diyne and the subsequent Scholl reaction forming the [8]circulene moiety. Two incompletely cyclized products were isolated from the Scholl reaction, providing insight into the cyclization of the strained octagon. This nanographene is twisted along two directions with end-to-end twists of 142.4° and 140.2° as revealed by X-ray crystallography, and is flexible at room temperature as found from the computational and experimental studies.

Realizing n-Type Field-Effect Performance via Introducing Trifluoromethyl Groups into the Donor-Acceptor Copolymer Backbone

Developing a new strategy to obtain n-type organic semiconductors is crucial for the advance of organic electronics. We herein report the synthesis and investigation of a series of donor-acceptor-type diazaisoindigo-based copolymers, named PAIID-TFBVB-C1,

Synthesis of Pinacolylboronate-Substituted Stilbenes and their application to the synthesis of boron capped polyenes

A series of novel 4,4,5,5-tetramethyl-2-(4-substitutedstyrylphenyl)-1,3,2 dioxaborolane derivatives has been synthesized. 4-(4,4,5,5-tetramethyl-1,3,2-dioxaboratophenyl)-methyl triphenylphosphonium bromide (4) was treated with 3 equiv of tBuONa, various a