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3-Methanesulfonylaminophenylboronic acid, pinacol ester is a chemical compound that features a boronic acid functional group and a pinacol ester moiety. It is widely utilized in organic synthesis due to its reactivity and versatility in forming various chemical bonds.

305448-92-4

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305448-92-4 Usage

Uses

Used in Organic Synthesis:
3-Methanesulfonylaminophenylboronic acid, pinacol ester is used as a building block for the synthesis of biologically active molecules, pharmaceuticals, and agrochemicals. Its presence in Suzuki-Miyaura cross-coupling reactions allows for the formation of carbon-carbon and carbon-heteroatom bonds, which are crucial for creating complex organic structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Methanesulfonylaminophenylboronic acid, pinacol ester is used as a key intermediate in the development of new drugs. Its ability to form stable bonds with other molecules makes it a valuable component in the synthesis of potential therapeutic agents.
Used in Agrochemical Industry:
3-Methanesulfonylaminophenylboronic acid, pinacol ester is also employed in the agrochemical industry for the synthesis of various agrochemicals. Its role in creating stable and effective compounds contributes to the development of new pesticides and other agricultural products.
Used in Research and Development:
In the field of research and development, 3-Methanesulfonylaminophenylboronic acid, pinacol ester is used as a versatile tool for exploring new chemical reactions and bond formations. Its unique properties make it an essential component in the advancement of organic chemistry and the discovery of novel compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 305448-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,4,4 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 305448-92:
(8*3)+(7*0)+(6*5)+(5*4)+(4*4)+(3*8)+(2*9)+(1*2)=134
134 % 10 = 4
So 305448-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H20BNO4S/c1-12(2)13(3,4)19-14(18-12)10-7-6-8-11(9-10)15-20(5,16)17/h6-9,15H,1-5H3

305448-92-4 Well-known Company Product Price

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  • Aldrich

  • (636037)  3-(Methanesulfonylamino)phenylboronicacidpinacolester  97%

  • 305448-92-4

  • 636037-1G

  • 973.44CNY

  • Detail
  • Aldrich

  • (636037)  3-(Methanesulfonylamino)phenylboronicacidpinacolester  97%

  • 305448-92-4

  • 636037-5G

  • 3,469.05CNY

  • Detail

305448-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methylsulfonylaminophenylboronic acid, pinacol ester

1.2 Other means of identification

Product number -
Other names N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide

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:305448-92-4 SDS

305448-92-4Relevant academic research and scientific papers

BTK Inhibitors and uses thereof

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, (2020/05/02)

The invention discloses a bruton's tyrosine kinase (BTK) inhibitor and use thereof. Specifically, the invention provides heteroaromatic compounds or stereoisomers, geometrical isomers, tautomers, racemates, nitrogen oxides, hydrates, solvates, metabolites and pharmaceutically acceptable salts or prodrugs thereof, and pharmaceutical compositions containing the heteroaromatic compounds; the invention also discloses use of the heteroaromatic compounds or the pharmaceutical compositions containing the heteroaromatic compounds in preparation of medicines; the medicines can be used for treating autoimmune diseases, inflammatory diseases or proliferative diseases.

3-(PYRAZOLYL)-1H-PYRROLO[2,3-b]PYRIDINE DERIVATIVES AS KINASE INHIBITORS

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, (2014/01/18)

The present application relates to novel 3-(pyrazolyl)-lH-pyrrolo[2,3-b]pyridine derivatives of formula (I), as protein kinase inhibitors. The invention particularly relates to compounds of formula (I), preparation of compounds and pharmaceutical compositions thereof. The invention further relates to pharmaceutically acceptable salts and compositions comprising the said novel 3-(pyrazolyl)-lH-pyrrolo[2,3-b]pyridine derivatives and their use in the treatment of various disorders.

NOVEL COMPOUNDS AS MODULATORS OF PROTEIN KINASES

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Page/Page column 129; 130, (2012/11/14)

The present invention provides PI3K protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of kinase mediated diseases or disorders with them.

NOVEL COMPOUNDS AS MODULATORS OF PROTEIN KINASES

-

Page/Page column 113, (2012/12/13)

The present invention provides PI3K protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of kinase mediated diseases or disorders with them.

2-Amino-aryl-7-aryl-benzoxazoles as potent, selective and orally available JAK2 inhibitors

Gerspacher, Marc,Furet, Pascal,Pissot-Soldermann, Carole,Gaul, Christoph,Holzer, Philipp,Vangrevelinghe, Eric,Lang, Marc,Erdmann, Dirk,Radimerski, Thomas,Regnier, Catherine H.,Chene, Patrick,Pover, Alain De,Hofmann, Francesco,Baffert, Fabienne,Buhl, Thomas,Aichholz, Reiner,Blasco, Francesca,Endres, Ralf,Trappe, J?rg,Drueckes, Peter

scheme or table, p. 1724 - 1727 (2010/07/03)

A series of novel benzoxazole derivatives has been designed and shown to exhibit attractive JAK2 inhibitory profiles in biochemical and cellular assays, capable of delivering compounds with favorable PK properties in rats. Synthesis and structure-activity relationship data are also provided.

Preparation of Aminoaryl and Aminoheteroaryl Boronic Acids and Derivatives Thereof

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Page/Page column 6, (2008/12/04)

The invention relates to a method for preparation of aminoaryl- or aminoheteroarylboronic acids and esters and salts thereof in which an optionally substituted aminoaryl or aminoheteroaryl compound is protected at its nitrogen site via condensation with a carbonyl compound, subsequently metalated and converted with a suitable boron compound. Depending on the subsequent work-up and removal of the protective group, the corresponding boronic acid, the anhydride or the boronic acid ester thereof is obtained

Sulfonamide derivatives

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, (2010/02/05)

The present invention provides certain sulfonamide derivatives useful for potentiating glutamate receptor function in a patient and therefore, useful for treating a wide variety of conditions, such as psychiatric and neurological disorders.

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