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4-Cyanopyridine-3-boronic acid neopentyl glycol ester is a boronic acid derivative featuring a neopentyl glycol ester group, which is utilized in organic synthesis as a versatile building block for the preparation of diverse functionalized compounds. Its unique structure and reactivity, particularly in Suzuki-Miyaura cross-coupling reactions, make it a valuable asset in the synthesis of complex organic molecules for various applications.

868944-72-3

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868944-72-3 Usage

Uses

Used in Pharmaceutical Industry:
4-Cyanopyridine-3-boronic acid neopentyl glycol ester is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex molecular structures that can exhibit therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Cyanopyridine-3-boronic acid neopentyl glycol ester is employed as a precursor in the development of novel agrochemicals, leveraging its reactivity to form compounds with potential pesticidal or herbicidal activity.
Used in Organic Synthesis:
4-Cyanopyridine-3-boronic acid neopentyl glycol ester is used as a reagent in organic synthesis for its capacity to participate in a variety of chemical reactions, enabling the formation of a broad spectrum of organic molecules with specific functionalities.
Used in Fine Chemicals Production:
4-Cyanopyridine-3-boronic acid neopentyl glycol ester is also utilized as a building block in the production of fine chemicals, where its unique properties can be harnessed to create specialty chemicals for various high-value applications.

Check Digit Verification of cas no

The CAS Registry Mumber 868944-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,9,4 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 868944-72:
(8*8)+(7*6)+(6*8)+(5*9)+(4*4)+(3*4)+(2*7)+(1*2)=243
243 % 10 = 3
So 868944-72-3 is a valid CAS Registry Number.

868944-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)pyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-(5,5-dimethyl-[1,3,2]-dioxaborinan-2-yl)isonicotinonitrile

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:868944-72-3 SDS

868944-72-3Relevant academic research and scientific papers

Synthesis of azaphenanthridines via anionic ring closure

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

, p. 9955 - 9960 (2007/10/03)

A new and convergent synthesis of azaphenanthridines via an anionic ring closure is reported. Ortho-lithiation/in situ borylation of cyanopyridines produces the corresponding cyanopyridylboronic esters, which undergo a Suzuki-Miyaura cross-coupling to giv

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