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2-Cyano-3-Methoxyphenylboronic Acid Neopentyl Glycol Ester is a boronic acid derivative featuring a cyano and methoxy group attached to a phenyl ring. It is the ester of neopentyl glycol and 2-Cyano-3-Methoxyphenylboronic Acid, serving as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and materials.

883899-02-3

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883899-02-3 Usage

Uses

Used in Organic Synthesis:
2-Cyano-3-Methoxyphenylboronic Acid Neopentyl Glycol Ester is used as a building block for the preparation of various pharmaceuticals, agrochemicals, and materials. Its unique structure allows for the formation of carbon-carbon bonds in organic compounds, making it a valuable component in the synthesis of complex organic molecules.
Used in Suzuki-Miyaura Coupling Reactions:
In the field of organic chemistry, 2-Cyano-3-Methoxyphenylboronic Acid Neopentyl Glycol Ester is utilized as a reagent in Suzuki-Miyaura coupling reactions. These reactions are significant for the formation of carbon-carbon bonds in organic compounds, enabling the creation of a wide range of organic molecules with potential applications in various industries.
Used in Optoelectronic Devices Development:
2-Cyano-3-Methoxyphenylboronic Acid Neopentyl Glycol Ester has potential applications in the development of optoelectronic devices, such as organic light-emitting diodes (OLEDs). Its unique properties make it a promising candidate for improving the performance and efficiency of these devices.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Cyano-3-Methoxyphenylboronic Acid Neopentyl Glycol Ester is used as a key intermediate in the synthesis of various drugs. Its ability to form carbon-carbon bonds and its unique structural features make it a valuable component in the development of new pharmaceutical compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Cyano-3-Methoxyphenylboronic Acid Neopentyl Glycol Ester is used as a building block for the synthesis of various agrochemicals, such as pesticides and herbicides. Its versatility in organic synthesis allows for the development of new and more effective agrochemicals to protect crops and enhance agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 883899-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,8,9 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 883899-02:
(8*8)+(7*8)+(6*3)+(5*8)+(4*9)+(3*9)+(2*0)+(1*2)=243
243 % 10 = 3
So 883899-02-3 is a valid CAS Registry Number.

883899-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)-6-methoxybenzonitrile

1.2 Other means of identification

Product number -
Other names 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-6-methoxybenzonitrile

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:883899-02-3 SDS

883899-02-3Relevant academic research and scientific papers

Novel syntheses of fluorenones via nitrile-directed palladium-catalyzed C-H and dual C-H bond activation

Wan, Jung-Chih,Huang, Jun-Min,Jhan, Yu-Huei,Hsieh, Jen-Chieh

supporting information, p. 2742 - 2745 (2013/07/19)

Novel procedures for the [Pd]/[Ag]/TFA system catalyzed cascade reactions of nitrile directed remote C-H and dual C-H bond activation with insertion of nitrile were developed, which afforded variously polysubstituted fluorenones in moderate to good yields with tolerance of a wide variety of substrates.

Synthesis of substituted 2-cyanoarylboronic esters

Lysen, Morten,Hansen, Henriette M.,Begtrup, Mikael,Kristensen, Jesper L.

, p. 2518 - 2520 (2007/10/03)

The synthesis of substituted 2-cyanoarylboronic esters is described via lithiation/in situ trapping of the corresponding methoxy-, trifluoromethyl-, fluoro-, chloro-, and bromobenzonitriles. The crude arylboronic esters were obtained in high yields and pu

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