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548797-51-9

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548797-51-9 Usage

General Description

2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile is a chemical compound noted for its complex structure. It belongs to the class of organoboron compounds, more specifically to the group of dioxaborolanes. As indicated by its name, it features a benzene ring attached to a nitrile group and a chloro-substituent, as well as a dioxaborolane ring. The dioxaborolane ring is characterized by two oxygen atoms and a boron atom, and the presence of four methyl groups. 2-Chloro-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzonitrile is typically used in scientific research, particularly in the field of organic synthesis. It may be used as a reagent in Suzuki-Miyaura coupling reactions, which are widely used in the formation of carbon-carbon bonds.

Check Digit Verification of cas no

The CAS Registry Mumber 548797-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,7,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 548797-51:
(8*5)+(7*4)+(6*8)+(5*7)+(4*9)+(3*7)+(2*5)+(1*1)=219
219 % 10 = 9
So 548797-51-9 is a valid CAS Registry Number.

548797-51-9SDS

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-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names -

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:548797-51-9 SDS

548797-51-9Relevant articles and documents

Facile synthesis of benzobisimidazole and bibenzimidazole-based bisnitriles as potential precursors for DNA minor groove binders

Farahat, Abdelbasset A.,Iwamoto, Satori,Roche, Michael,Boykin, David W.

, p. 2280 - 2286 (2021/08/16)

The synthesis of bisnitrile derivatives of benzobisimidazole and bibenzimidazole in a good yield is described in detail for the first time. Nucleophilic substitution of 1,5-difluoro-2,4-dinitrobenzene using different amines produced the intermediate diami

ALKYNE COMPOUNDS AS S-NITROSOGLUTATHIONE REDUCTASE INHIBITORS

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Page/Page column 76; 77; 86; 87, (2016/05/02)

Provided are compounds of formula (Ia) and pharmaceutically acceptable salts thereof, wherein A, B, R 1, R 2, m and n are as defined herein, which are active as inhibitors of S-Nitrosoglutathione reductase (GSNOR). These compounds prevent, inhibit, or suppress the action of GSNOR and are therefore useful in the treatment of GSNOR mediated diseases, disorders, syndromes or conditions such as, e.g., pulmonary hypertension, acute respiratory distress syndrome (ARDS), asthma, bronchospasm, cough, pneumonia, pulmonary fibrosis, interstitial lung diseases, cystic fibrosis and chronic obstructive pulmonary disease (COPD).

ARYL PYRIDINE AS ALDOSTERONE SYNTHASE INHIBITORS

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Page/Page column 57, (2012/04/23)

The present invention provides a compound of Formula (I); a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

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