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886547-94-0

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  • 1-(Phenylsulfonyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolo[2,3-b]pyridine

    Cas No: 886547-94-0

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886547-94-0 Usage

General Description

1-(Benzenesulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-boronic acid pinacol ester is a complex and highly specific type of organic compound. As a boronic ester, this substance features boron and oxygen atoms, and is often used in the formation of other complex compounds through catalytic or stoichiometric processes. Its structure also features a pyrrolopyridine core, which is a biologically significant scaffold found in various pharmaceutical agents due to its unique photophysical properties and ability to create diverse molecular architectures. In addition, it has a benzenesulfonyl group, contributing to its overall stability and reactivity. It is likely that this chemical is used in advanced scientific research, specifically in fields like organic chemistry and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 886547-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 886547-94:
(8*8)+(7*8)+(6*6)+(5*5)+(4*4)+(3*7)+(2*9)+(1*4)=240
240 % 10 = 0
So 886547-94-0 is a valid CAS Registry Number.
InChI:InChI=1S/C19H27BN2O4/c1-12-14-11-13(20-25-18(5,6)19(7,8)26-20)9-10-15(14)22(21-12)16(23)24-17(2,3)4/h9-11H,1-8H3

886547-94-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H31505)  1-Phenylsulfonyl-7-azaindole-3-boronic acid pinacol ester, 95%   

  • 886547-94-0

  • 250mg

  • 4733.0CNY

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  • Aldrich

  • (735019)  1-(Phenylsulfonyl)-7-azaindole-3-boronic acid pinacol ester  95%

  • 886547-94-0

  • 735019-250MG

  • 896.22CNY

  • Detail
  • Aldrich

  • (735019)  1-(Phenylsulfonyl)-7-azaindole-3-boronic acid pinacol ester  95%

  • 886547-94-0

  • 735019-1G

  • 2,798.64CNY

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886547-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Benzenesulfonyl)-1H-Pyrrolo[2,3-b]Pyridine-3-Boronic Acid Pinacol Ester

1.2 Other means of identification

Product number -
Other names 1-(benzenesulfonyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolo[2,3-b]pyridine

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:886547-94-0 SDS

886547-94-0Relevant articles and documents

Discovery of 1,8-disubstituted-[1,2,3]triazolo[4,5-c]quinoline derivatives as a new class of Hippo signaling pathway inhibitors

Chen, Pei,Li, L.,Lin, Guifeng,Qiao, Jingxin,Xia, A.,Xiang, Z.,Yang, Shengyong,Zhang, Guo

supporting information, (2019/08/12)

Inhibitors of the Hippo signaling pathway have been demonstrated to have a potential clinical application in cases such as tissue repair and organ regeneration. However, there is a lack of potent Hippo pathway inhibitors at present. Herein we report the discovery of a series of 1,8-disubstituted-[1,2,3]triazolo[4,5-c]quinoline derivatives as a new class of Hippo pathway inhibitors by utilizing a cell line-based screening model (A549-CTGF). Structure-activity relationship (SAR) of these compounds was also discussed. The most potent compound in the A549-CTGF cell assay, 11g, was then evaluated by real-time PCR and immunofluorescence assays. Overall, this study provides a starting point for later drug discovery targeting the Hippo signaling pathway.

PHTHALAZIN-(2H)-ONE INHIBITORS OF KINASES

-

Page/Page column 22, (2011/10/31)

The present invention relates to compounds of formula (I) or pharmaceutical acceptable salts, wherein R1a, R1b, R1c, X, Y, Z, n, and m are defined in the description. The present invention relates also to compositions cont

PYRIDINONYL PDK1 INHIBITORS

-

Page/Page column 103, (2008/06/13)

The present invention provides pyridinonyl PDKl inhibitors and methods of treating cancer using the same.

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