65423-56-5

Basic information

• Product Name: 1-BROMO-3-(TERT-BUTYLDIMETHYLSILOXY)BENZENE
• Synonyms: Benzene, 1-broMo-3-[[(1,1-diMethylethyl)diMethylsilyl]oxy]-;[(3-BroMophenyl)oxy](1,1-diMethylethyl)diMethylsilane;1-BroMo-3-[[(1,1-diMethylethyl)diMethylsilyl]oxy]-benzene;1-BroMo-3-tert-butyldiMethylsilyloxybenzene;3-(tert-Bu;3-BroMophenyl tert-ButyldiMethylsilyl Ether;(3-BroMophenoxy)(tert-butyl)diMethylsilane;(3-Bromophenoxy)-t-Butyl-Dimethylsilane
• CAS NO: 65423-56-5
• Molecular Formula: C₁₂H₁₉BrOSi
• Molecular Weight: 287.27
• EINECS: -0
• Product Categories: Aromatics;Inhibitors
• Mol File: 65423-56-5.mol
• Article Data: 38

Chemical Properties

• Boiling Point: 66°C 0,3mm
• Flash Point: 66°C/0.3mm
• Appearance: /
• Density: 1.158g/cm³
• Vapor Pressure: 0.0156mmHg at 25°C
• Refractive Index: 1.5090
• Storage Temp.: 2-8°C
• Solubility: Chloroform, DIchloromethane, Ethyl Acetate
• Sensitive: Moisture Sensitive
• BRN: 2256298
• CAS DataBase Reference: 1-BROMO-3-(TERT-BUTYLDIMETHYLSILOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-3-(TERT-BUTYLDIMETHYLSILOXY)BENZENE(65423-56-5)
• EPA Substance Registry System: 1-BROMO-3-(TERT-BUTYLDIMETHYLSILOXY)BENZENE(65423-56-5)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 65423-56-5(Hazardous Substances Data)

Usage

Chemical Properties

Colorless OIl

Uses

Enzyme inhibitor.

InChI:InChI=1/C12H19BrOSi/c1-12(2,3)15(4,5)14-11-8-6-7-10(13)9-11/h6-9H,1-5H3

Upstream product

• 108-36-1 1,3-dibromobenzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 136386-79-3 (3,5-dibromophenoxy)-tert-butyldimethylsilane 
• 1123-89-3 2-Methyl-phenylcyanat 
• 288-32-4 1H-imidazole 
• 591-20-8 3-Bromophenol 

Downstream Products

• 155767-23-0 α-(3-bromophenyl)-3-(tert-butyldimethylsilyloxy)-benzyl alcohol 
• 199938-29-9 1-(tert-butyloxycarbonyl)-4-[3-{3-(tert-butyldimethylsilyloxy)phenyl}-3-hydroxy-3-phenylpropyl]homopiperazine 
• 850664-15-2 4-(3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}phenyl)-4-oxobutanoic acid 
• 868694-00-2 5-bromo-2-(3-t-butyldimethylsilyloxy-benzoyl)-benzoic acid 
• 868693-98-5 4-bromo-2-(3-t-butyldimethylsilyloxy-benzoyl)-benzoic acid 
• 1254224-06-0 tert-butyl (S)-(3-(3-((tert-butyldimethylsilyl)oxy)phenyl)but-3-en-2-yl)carbamate 
• 1301205-26-4 7-hydroxy-5,5-dimethyl-10-(o-tolyl)dibenzo[b,e]silin-3(5H)-one 

Relevant articles and documents

ANTIVIRAL 1,3-DI-OXO-INDENE COMPOUNDS

This disclosure provides compounds of Formula (I) as described herein, along with pharmaceutically acceptable salts, pharmaceutical compositions containing such compounds, and methods to use these compounds, salts and compositions for treating viral infections.

SELECTIVE FLUORESCENT PROBE FOR ALDEHYDE DEHYDROGENASE

High aldehyde dehydrogenase 1A1 (ALDH1A1) activity has emerged as a reliable marker for the identification of both normal and cancer stem cells. Herein, is presented AlDeSense, a turn-on green fluorescent probe for aldehyde dehydrogenase 1A1 (ALDH1A1) and Ctrl-AlDeSense, a matching non-responsive reagent. AlDeSense exhibits a 20-fold fluorescent enhancement when treated with ALDH1A1. Through the application of surface marker antibody staining, tumorsphere assays, and assessment of tumorigenicity, the disclosed results show that cells exhibiting high AlDeSense signal intensity have properties of cancer stem cells. Herein, is also reported the development of a red congener, red-AlDeSense. Importantly, red-AlDeSense represents one of only a few examples of a turn-on sensor in the red region using the d-PeT quenching mechanism.

Colored curable resin composition

The present invention addresses the problem of providing a colored curable resin composition with which it is possible to form a color filter that exhibits superior light-absorbency retention rate. The present invention relates to a colored curable resin composition comprising a colorant, a resin, a polymerizable compound and a polymerization initiator, wherein the colorant includes a squarylium dye represented by formula (I), and the resin includes a structural unit derived from an N-substituted maleimide.