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885069-14-7

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885069-14-7 Usage

General Description

N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamide is a chemical compound that belongs to the class of acetamides. It contains a benzothiazole moiety with a boron-containing functional group attached to it. N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamide has potential applications in medicinal chemistry as a building block for the synthesis of pharmaceuticals or bioactive molecules. The presence of the boron-containing group makes it useful for cross-coupling reactions, which are widely used in organic synthesis. Additionally, the benzothiazole moiety is found in various pharmacologically active compounds, suggesting potential biological activities for N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazol-2-yl)acetamide. Further exploration of its properties and potential applications is warranted.

Check Digit Verification of cas no

The CAS Registry Mumber 885069-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,0,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885069-14:
(8*8)+(7*8)+(6*5)+(5*0)+(4*6)+(3*9)+(2*1)+(1*4)=207
207 % 10 = 7
So 885069-14-7 is a valid CAS Registry Number.

885069-14-7SDS

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 Acetamide, N-[6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-benzothiazolyl]-

1.2 Other means of identification

Product number -
Other names N-[6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzothiazol-2-yl]acetamide

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:885069-14-7 SDS

885069-14-7Relevant articles and documents

HETEROARYL COMPOUNDS AS INHIBITORS OF NECROSIS, COMPOSITION AND APPLICATION THEREOF

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, (2018/02/20)

The present disclosure provides heteroaryl compounds of formulas (I), (Ia) and (Ib), processes for their preparation, pharmaceutical compositions containing them, and their use in the treatment of diseases and disorders, arising from or related to necrosi

MECHANISTIC TARGET OF RAPAMYCIN SIGNALING PATHWAY INHIBITORS AND THERAPEUTIC APPLICATIONS THEREOF

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, (2018/04/11)

Selective mTOR inhibitors of formulas (I)-(III), processes for their preparation, pharmaceutical compositions containing them, and their use in the treatment of diseases and disorders, arising from abnormal cell growth, functions, or behaviors mediated by an mTOR kinase and/or one or more PI3K enzyme, are provided. Such diseases and disorder include cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine function disorders and neurological disorders.

Structural basis for isoform selectivity in a class of benzothiazole inhibitors of phosphoinositide 3-kinase γ

Collier, Philip N.,Martinez-Botella, Gabriel,Cornebise, Mark,Cottrell, Kevin M.,Doran, John D.,Griffith, James P.,Mahajan, Sudipta,Maltais, Fran?ois,Moody, Cameron S.,Huck, Emilie Porter,Wang, Tiansheng,Aronov, Alex M.

, p. 517 - 521 (2015/02/19)

Phosphoinositide 3-kinase γ (PI3Kγ) is an attractive target to potentially treat a range of disease states. Herein, we describe the evolution of a reported phenylthiazole pan-PI3K inhibitor into a family of potent and selective benzothiazole inhibitors. U

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