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1-BROMO-3-(TERT-BUTYLDIMETHYLSILOXY)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65423-56-5

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65423-56-5 Usage

Chemical Properties

Colorless OIl

Uses

Enzyme inhibitor.

Check Digit Verification of cas no

The CAS Registry Mumber 65423-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,2 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65423-56:
(7*6)+(6*5)+(5*4)+(4*2)+(3*3)+(2*5)+(1*6)=125
125 % 10 = 5
So 65423-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H19BrOSi/c1-12(2,3)15(4,5)14-11-8-6-7-10(13)9-11/h6-9H,1-5H3

65423-56-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L17440)  1-Bromo-3-(tert-butyldimethylsiloxy)benzene, 98+%   

  • 65423-56-5

  • 1g

  • 323.0CNY

  • Detail
  • Alfa Aesar

  • (L17440)  1-Bromo-3-(tert-butyldimethylsiloxy)benzene, 98+%   

  • 65423-56-5

  • 5g

  • 1095.0CNY

  • Detail

65423-56-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-bromophenoxy)-tert-butyl-dimethylsilane

1.2 Other means of identification

Product number -
Other names 3-bromophenyl tert-butyldimethylsilyl ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65423-56-5 SDS

65423-56-5Relevant academic research and scientific papers

ANTIVIRAL 1,3-DI-OXO-INDENE COMPOUNDS

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Paragraph 0267-0268, (2021/10/22)

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.

A Photoactivatable Formaldehyde Donor with Fluorescence Monitoring Reveals Threshold to Arrest Cell Migration

Chan, Jefferson,Ibarra, Gabriela E.,Krishnamurthy, Vishnu,Pino, Nicholas W.,Smaga, Lukas P.

supporting information, (2020/01/31)

Controlled light-mediated delivery of biological analytes can enable the investigation of highly reactivity molecules within living systems. As many biological effects are concentration dependent, it is critical to determine the location, time, and quantity of analyte donation. In this work, we have developed the first photoactivatable donor for formaldehyde (FA). Our optimized photoactivatable donor, photoFAD-3, is equipped with a fluorescence readout that enables monitoring of FA release with a concomitant 139-fold fluorescence enhancement. Tuning of photostability and cellular retention enabled quantification of intracellular FA release through cell lysate calibration. Application of photoFAD-3 uncovered the concentration range necessary for arresting wound healing in live cells. This marks the first report where a photoactivatable donor for any analyte has been used to quantify intracellular release.

SELECTIVE FLUORESCENT PROBE FOR ALDEHYDE DEHYDROGENASE

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Paragraph 0247, (2020/07/14)

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

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Paragraph 0155-0157, (2021/02/24)

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.

Synthesis of Trisubstituted Alkenyl Boronic Esters from Alkenes Using the Boryl-Heck Reaction

Reid, William B.,Watson, Donald A.

supporting information, p. 6832 - 6835 (2018/10/24)

The direct borylation of disubstituted alkenes is reported. These conditions allow for the conversion of a variety 1,1- and 1,2-disubstituted alkenes to trisubstituted alkenyl boronic esters with outstanding yields and excellent E/Z selectivities. The utility of this reaction has been demonstrated with several downstream functionalization reactions, which allow access to diverse, stereodefined, functionalized olefins. Mechanistic studies are consistent with a boryl-Heck pathway.

AN OPIOID FOR USE TO REDUCE AND/OR TREAT DRUG ADDICTION

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Paragraph 0078; 0080, (2018/11/26)

The present invention relates to a method of treating drug addiction and reducing dependence or tolerance on a dependence-inducing opiate drug, wherein the method comprises administering to a subject a compound having the structure of formula (I): having

Synthesis of C2 Substituted Benzothiophenes via an Interrupted Pummerer/[3,3]-Sigmatropic/1,2-Migration Cascade of Benzothiophene S-Oxides

He, Zhen,Shrives, Harry J.,Fernández-Salas, José A.,Abengózar, Alberto,Neufeld, Jessica,Yang, Kevin,Pulis, Alexander P.,Procter, David J.

supporting information, p. 5759 - 5764 (2018/04/10)

Functionalized benzothiophenes are important scaffolds found in molecules with wide ranging biological activity and in organic materials. We describe an efficient, metal-free synthesis of C2 arylated, allylated, and propargylated benzothiophenes. The reaction utilizes synthetically unexplored yet readily accessible benzothiophene S-oxides and phenols, allyl-, or propargyl silanes in a unique cascade sequence. An interrupted Pummerer reaction between benzothiophene S-oxides and the coupling partners yields sulfonium salts that lack aromaticity and therefore allow facile [3,3]-sigmatropic rearrangement. The subsequently generated benzothiophenium salts undergo a previously unexplored 1,2-migration to access C2 functionalized benzothiophenes.

DELTA OPIOID AGONIST, MU OPIOID ANTAGONIST COMPOSITIONS AND METHODS FOR TREATING PARKINSON'S DISEASE

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Page/Page column 19; 20, (2017/11/04)

The present invention provides for compositions and methods for the treatment of Parkinson's disease comprising a compound of formula (i): or a pharmaceutically effective salt or ester thereof alone or in combination with L-DOPA to provide a synergistic e

COMPOSITIONS AND METHODS FOR INHIBITION OF CATHEPSINS

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Paragraph 0153; 0154; 0155, (2017/03/14)

This present disclosure is directed to compound of Formula I and methods of using these compounds in the treatment of conditions in which modulation of a cathepsin, particularly cathepsin L, cathepsin K, and/or cathepsin B, will be therapeutically useful.

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