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945391-06-0

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945391-06-0 Usage

Description

2-Chloro-4-cyanophenylboronic Acid Pinacol Ester is a chemical compound with the molecular formula C12H12BClNO2. It is a boronic acid ester derivative that is commonly used in organic synthesis and pharmaceutical research. 2-Chloro-4-cyanophenylboronic Acid Pinacol Ester is known for its ability to react with various organic compounds, making it a versatile building block for the synthesis of complex molecules.

Uses

Used in Pharmaceutical Research:
2-Chloro-4-cyanophenylboronic Acid Pinacol Ester is used as a key intermediate in the development of new drugs. Its reactivity allows for the creation of complex molecular structures that can be tailored for specific therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 2-Chloro-4-cyanophenylboronic Acid Pinacol Ester is used as a building block for the synthesis of novel compounds with pesticidal properties. Its versatility in organic synthesis enables the design of molecules with improved efficacy and selectivity.
Used in Material Science:
2-Chloro-4-cyanophenylboronic Acid Pinacol Ester is utilized in the development of materials with specific properties. Its ability to form stable linkages with other molecules allows for the creation of materials with tailored characteristics, such as improved mechanical strength or unique electronic properties.
Overall, 2-Chloro-4-cyanophenylboronic Acid Pinacol Ester is a valuable compound in the fields of chemistry and biochemistry, with a wide range of potential applications in scientific research and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 945391-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,3,9 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 945391-06:
(8*9)+(7*4)+(6*5)+(5*3)+(4*9)+(3*1)+(2*0)+(1*6)=190
190 % 10 = 0
So 945391-06-0 is a valid CAS Registry Number.

945391-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chloro-4-cyanophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-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:945391-06-0 SDS

945391-06-0Downstream Products

945391-06-0Relevant articles and documents

Zig-Zag Type Molecular Design Strategy of N-Type Hosts for Sky-Blue Thermally-Activated Delayed Fluorescence Organic Light-Emitting Diodes

Yang, Chang Yoon,Lee, Kyung Hyung,Lee, Jun Yeob

supporting information, p. 2429 - 2435 (2020/02/13)

N-type hosts for long lifetime in sky-blue thermally-activated delayed fluorescence (TADF) organic light-emitting diodes (OLEDs) were investigated by synthesizing four hosts with zig-zag-type backbone structure for high triplet energy. The four hosts had

CONDENSED RING DERIVATIVE, AND PREPARATION METHOD, INTERMEDIATE, PHARMACEUTICAL COMPOSITION AND USE THEREOF

-

Paragraph 0206; 0207, (2018/02/28)

Disclosed are a condensed ring derivative, and a preparation method, an intermediate, a pharmaceutical composition and a use thereof. The condensed ring derivative of the present invention has a significant inhibitive effect on URAT1, which can effectively alleviate or treat hyperuricemia and other related diseases.

Synthesis of ladder-type π-conjugated heteroacenes via palladium-catalyzed double N-arylation and intramolecular O-arylation

Kawaguchi, Keiko,Nakano, Koji,Nozaki, Kyoko

, p. 5119 - 5128 (2008/02/07)

(Chemical Equation Presented) Ladder-type heteroacenes containing pyrrole or furan rings, indolo[3,2-b]carbazoles and dibenzo[d,d′]-benzo[1,2-b:4,5- b′]difurans, were effectively synthesized from the common intermediates, 2,5-bis(o-chloroaryl)hydroquinones. The key reactions are palladium-catalyzed double N-arylation of aniline and intramolecular O-arylation, which enable regioselective ring closure. In addition to the parent indolo[3,2-b]carbazole and dibenzo[d,d′]benzo[1,2-b:4,5-b′]difuran, their derivatives with an alkyl or cyano group were first synthesized. Photophysical and electrochemical studies showed that the obtained heteroacenes have lower HOMO energy levels and larger band gaps than the corresponding hydrocarbon acene, pentacene. An X-ray analysis of dibenzo[d,d′]benzo[1,2-b:4,5-b′] difuran revealed that it was packed in herringbone fashion.

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