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400620-72-6

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400620-72-6 Usage

General Description

2-Dioxaborolan-2-yl)quinolin-2(1H)-one, also known as quinolin-2(1H)-one, is a chemical compound with the molecular formula C10H7BO2. It is a heterocyclic compound that contains both boron and oxygen atoms in its structure. 2-dioxaborolan-2-yl)quinolin-2(1H)-one has been studied for its potential applications in organic synthesis and pharmaceutical research, as it can be used as a building block for the synthesis of functionalized quinolin-2(1H)-one derivatives. These derivatives have shown promise in various biological and medicinal activities, such as antimicrobial, anti-inflammatory, and anticancer properties. Additionally, quinolin-2(1H)-one derivatives have been investigated for their potential as enzyme inhibitors and neuroprotective agents. Overall, this chemical compound has generated interest in the scientific community for its diverse potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 400620-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,6,2 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 400620-72:
(8*4)+(7*0)+(6*0)+(5*6)+(4*2)+(3*0)+(2*7)+(1*2)=86
86 % 10 = 6
So 400620-72-6 is a valid CAS Registry Number.

400620-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-1H-qu inolin-2-one

1.2 Other means of identification

Product number -
Other names 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one

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:400620-72-6 SDS

400620-72-6Relevant articles and documents

Pd-Catalyzed Site-Selective Borylation of Simple Arenes via Thianthrenation?

Chen, Xiao-Yue,Huang, Yu-Hao,Zhou, Jian,Wang, Peng

, p. 1269 - 1272 (2020/08/13)

Site-selective borylation of simple arenes was realized in one pot via an electrophilic thianthrenation/Pd-catalyzed borylation sequence. The key to achieve this operatically simple process is the use of Pd catalysis, which could tolerate the solvent and acidic conditions used in the thianthrenation step. This protocol features mild conditions, broad functional group tolerance, and simple manipulations, and is suitable for late-stage functionalization of a wide range of pharmaceuticals and complex bioactive molecules.

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