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2-Methyl-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanenitrile is a pyridine derivative with a molecular formula of C15H20BN2O2. It is characterized by the presence of a boron atom and a nitrile group, which contribute to its unique chemical properties. 2-Methyl-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanenitrile is of interest in the realm of organic synthesis, particularly for its role in the formation of carbon-carbon and carbon-heteroatom bonds.

1402390-59-3

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1402390-59-3 Usage

Uses

Used in Organic Synthesis:
2-Methyl-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanenitrile is used as a reagent in cross-coupling reactions for the creation of complex organic molecules. Its ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it a valuable component in the synthesis of a variety of organic compounds.
Used in Material Science:
The boron-containing structure of 2-Methyl-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanenitrile also lends itself to the development of boron-based materials. It can be utilized in the creation of materials with specific properties, such as those with enhanced thermal stability or unique electronic characteristics, for applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Methyl-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanenitrile is used as a building block for the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
2-Methyl-2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propanenitrile is also used in chemical research as a model compound to study the reactivity and properties of boron-containing organic molecules. This research can lead to a better understanding of the role of boron in organic chemistry and the development of new synthetic methods and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1402390-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,3,9 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1402390-59:
(9*1)+(8*4)+(7*0)+(6*2)+(5*3)+(4*9)+(3*0)+(2*5)+(1*9)=123
123 % 10 = 3
So 1402390-59-3 is a valid CAS Registry Number.

1402390-59-3SDS

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 2-Methyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyr idinyl]propanenitrile

1.2 Other means of identification

Product number -
Other names Dactolisib Tosylate

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:1402390-59-3 SDS

1402390-59-3Relevant academic research and scientific papers

AMINOPYRAZINE COMPOUNDS USEFUL AS INHIBITORS OF TRA KINASE

-

, (2012/10/18)

The present invention relates to compounds useful as inhibitors of ATR protein kinase. The invention also relates to pharmaceutically acceptable compositions comprising the compounds of this invention; methods of treating of various diseases, disorders, and conditions using the compounds of this invention; processes for preparing the compounds of this invention; intermediates for the preparation of the compounds of this invention; and methods of using the compounds in in vitro applications, such as the study of kinases in biological and pathological phenomena; the study of intracellular signal transduction pathways mediated by such kinases; and the comparative evaluation of new kinase inhibitors. The compounds of this invention have formula (I): wherein the variables are as defined herein.

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