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(3-BROMOPHENOXY)TRIISOPROPYLSILANE 97 is a trialkylsilyl halide derivative that serves as a crucial reagent in organic synthesis. It is recognized for its role in the preparation of a variety of organic compounds, including pharmaceutical drugs, agrochemicals, and other biologically active molecules. Its versatility and importance in the field of organic chemistry make it a valuable component in both industrial and academic research.

571202-87-4

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571202-87-4 Usage

Uses

Used in Pharmaceutical Industry:
(3-BROMOPHENOXY)TRIISOPROPYLSILANE 97 is used as a reagent for the synthesis of various pharmaceutical drugs. It aids in the preparation of biologically active molecules that can be utilized for the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, (3-BROMOPHENOXY)TRIISOPROPYLSILANE 97 is employed as a reagent for the synthesis of agrochemicals. It contributes to the development of compounds that can be used in the production of pesticides, herbicides, and other agricultural chemicals to enhance crop protection and yield.
Used in Polymer and Material Production:
(3-BROMOPHENOXY)TRIISOPROPYLSILANE 97 is used as a reagent in the production of various polymers and materials. Its application in this field allows for the creation of new materials with specific properties, such as improved strength, flexibility, or chemical resistance, which can be utilized in a wide range of industries.
Used in Academic and Industrial Research:
(3-BROMOPHENOXY)TRIISOPROPYLSILANE 97 is utilized as a reagent in academic and industrial research settings. Its role in the synthesis of organic compounds makes it an essential tool for scientists and researchers working on the development of new chemical processes, materials, and products.

Check Digit Verification of cas no

The CAS Registry Mumber 571202-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,1,2,0 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 571202-87:
(8*5)+(7*7)+(6*1)+(5*2)+(4*0)+(3*2)+(2*8)+(1*7)=134
134 % 10 = 4
So 571202-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H25BrOSi/c1-11(2)18(12(3)4,13(5)6)17-15-9-7-8-14(16)10-15/h7-13H,1-6H3

571202-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-bromophenoxy)-tri(propan-2-yl)silane

1.2 Other means of identification

Product number -
Other names 1-bromo-3-(triisopropylsilyloxy)benzene

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:571202-87-4 SDS

571202-87-4Relevant articles and documents

CELL-PENETRATING FLUORESCENT DYES WITH SECONDARY ALCOHOL FUNCTIONALITIES

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Page/Page column 31; 65; 66, (2018/03/28)

The invention relates to novel cell-penetrating fluorescent dyes with with secondary alcohol functionalities having one of the following general formulae I-III and 4: The invention also relates to the use of these compounds for optical microscopy and imaging techniques.

Hydroxylated Fluorescent Dyes for Live-Cell Labeling: Synthesis, Spectra and Super-Resolution STED

Butkevich, Alexey N.,Belov, Vladimir N.,Kolmakov, Kirill,Sokolov, Viktor V.,Shojaei, Heydar,Sidenstein, Sven C.,Kamin, Dirk,Matthias, Jessica,Vlijm, Rifka,Engelhardt, Johann,Hell, Stefan W.

supporting information, p. 12114 - 12119 (2017/09/14)

Hydroxylated rhodamines, carbopyronines, silico- and germanorhodamines with absorption maxima in the range of 530–640 nm were prepared and applied in specific labeling of living cells. The direct and high-yielding entry to germa- and silaxanthones tolerates the presence of protected heteroatoms and may be considered for the syntheses of various sila- and germafluoresceins, as well as -rhodols. Application in stimulated emission depletion (STED) fluorescence microscopy revealed a resolution of 50–75 nm in one- and two-color imaging of vimentin-HaloTag fused protein and native tubulin. The established structure–property relationships allow for prediction of the spectral properties and the positions of spirolactone/zwitterion equilibria for the new analogues of rhodamines, carbo-, silico-, and germanorhodamines using simple additive schemes.

Total syntheses of murrayamine E, I, and K

Schuster, Christian,Julich-Gruner, Konstanze K.,Schnitzler, Heinrich,Hesse, Ronny,J?ger, Anne,Schmidt, Arndt W.,Kn?lker, Hans-Joachim

, p. 5666 - 5673 (2015/06/16)

We describe efficient synthetic routes to murrayamine A (mukoenine C), O-methylmurrayamine A, mahanine, O-methylmahanine, and murrayamine D and the first total syntheses of murrayamine E, I, and K. Key steps are a palladium-catalyzed construction of the carbazole framework and an annulation of the pyran ring, which is either catalyzed by phenylboronic acid or promoted by a Lewis acid.

Synthesis of prenyl- and geranyl-substituted carbazole alkaloids by DIBAL-H promoted reductive pyran ring opening of dialkylpyrano[3,2-a]carbazoles

Hesse, Ronny,Kataeva, Olga,Schmidt, Arndt W.,Knoelker, Hans-Joachim

supporting information, p. 9504 - 9509 (2014/08/18)

The DIBAL-H promoted reductive pyran ring opening of dialkylpyrano[3,2-a] carbazoles provides a direct access to a broad range of prenyl- and geranyl-substituted carbazoles. Formation of a pyran ring followed by reductive ring opening represents a new met

Total synthesis of 7- and 8-oxygenated pyrano[3,2-a]carbazole and pyrano[2,3-a]carbazole alkaloids via boronic acid-catalyzed annulation of the pyran ring

Julich-Gruner, Konstanze K.,Kataeva, Olga,Schmidt, Arndt W.,Knoelker, Hans-Joachim

supporting information, p. 8536 - 8540 (2014/07/21)

The boronic acid-catalyzed annulation of citral opens up a short route to oxygenated cyclized monoterpenoid pyranocarbazole alkaloids. Thus, murrayamine-D is available in only three steps and 55% overall yield from the corresponding carbazole precursor.

Synthesis of macrocyclic ketones exploiting palladium-catalyzed activation of carboxylic acids as an enabling step

Kapdi, Anant R.,Fairlamb, Ian J. S.

, p. 961 - 964 (2013/06/27)

The novel synthesis of macrocyclic arylketones via palladium-catalyzed cross-coupling of arylboronic acids and carboxylic acids, activated by the treatment with di(N-succinimidyl) carbonate, is disclosed. This allows the high yielding synthesis of various

PHENOXYALKANOIC ACID COMPOUND

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Page/Page column 37, (2008/06/13)

The present invention provides a compound represented by the formula: wherein each symbol is as defined in the specification. Since the compound of the present invention has superior hypoglycemic action and superior hypolipidemic action, it is useful as an agent for the prophylaxis or treatment of diabetes, hyperlipidemia, impaired glucose tolerance and the like.

Design and evaluation of novel nonsteroidal dissociating glucocorticoid receptor ligands

Shah, Nilesh,Scanlan, Thomas S.

, p. 5199 - 5203 (2007/10/03)

A novel class of phenylpyrazole fused Wieland-Miescher ketone derivatives are high affinity, receptor specific, selective modulators of glucocorticoid receptor (GR) function.

Non-steroidal ligands for the glucocorticoid receptor, compositions and uses thereof

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, (2008/06/13)

The invention provides non-steroidal ligands for the glucocorticoid receptor, methods for making non-steroidal ligands of the glucocorticoid receptor, compositions of non-steroidal ligands of the glucocorticoid receptor and methods of using non-steroidal

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