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3-Chloro-2-cyanophenylboronic acid neopentyl glycol ester is a versatile chemical compound that features a boronic acid group and a neopentyl glycol ester moiety. This unique structure endows it with the ability to participate in a range of chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and materials. Its boron-containing framework also opens up possibilities for applications in medicinal chemistry and diagnostics, due to its potential reactivity and functional group compatibility.

883899-06-7

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883899-06-7 Usage

Uses

Used in Organic Synthesis:
3-Chloro-2-cyanophenylboronic acid neopentyl glycol ester serves as a key building block in the synthesis of various organic compounds. Its presence facilitates the creation of complex molecular structures that are essential in the development of new pharmaceuticals and agrochemicals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3-chloro-2-cyanophenylboronic acid neopentyl glycol ester is utilized as a precursor for the synthesis of drug candidates. Its ability to engage in Suzuki-Miyaura cross-coupling reactions and other boron-based transformations allows for the construction of diverse and bioactive molecules, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Production:
3-Chloro-2-cyanophenylboronic acid neopentyl glycol ester is also applied in the agrochemical sector, where it is used to synthesize new pesticides and herbicides. Its reactivity and structural features enable the development of more effective and environmentally friendly agrochemicals.
Used in Material Science:
In the field of material science, 3-chloro-2-cyanophenylboronic acid neopentyl glycol ester is employed in the design and synthesis of functional materials. Its boron-containing structure can be integrated into materials with unique electronic, optical, or mechanical properties, broadening its utility in various applications.
Used in Diagnostics:
3-Chloro-2-cyanophenylboronic acid neopentyl glycol ester's potential applications extend to diagnostics, where its boron-containing framework can be exploited for the development of diagnostic agents or imaging probes, enhancing the detection and monitoring of diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 883899-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,8,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 883899-06:
(8*8)+(7*8)+(6*3)+(5*8)+(4*9)+(3*9)+(2*0)+(1*6)=247
247 % 10 = 7
So 883899-06-7 is a valid CAS Registry Number.

883899-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzonitrile

1.2 Other means of identification

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

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:883899-06-7 SDS

883899-06-7Downstream Products

883899-06-7Relevant academic research and scientific papers

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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