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49568-68-5

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49568-68-5 Usage

General Description

3-Chloroquinoxaline-2-carbaldehyde is a chemical compound that belongs to the quinoxaline family. It is an aldehyde derivative with a chlorine atom attached to the third position of the quinoxaline ring. 3-CHLOROQUINOXALINE-2-CARBALDEHYDE has been synthesized as a key intermediate for the preparation of various pharmaceuticals and organic molecules. It is used in the synthesis of potential antifungal and antibacterial agents, as well as in the development of novel drugs for the treatment of various diseases. Additionally, 3-Chloroquinoxaline-2-carbaldehyde has also been studied for its potential use in the field of organic electronics and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 49568-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,6 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 49568-68:
(7*4)+(6*9)+(5*5)+(4*6)+(3*8)+(2*6)+(1*8)=175
175 % 10 = 5
So 49568-68-5 is a valid CAS Registry Number.

49568-68-5SDS

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-chloroquinoxaline-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-QUINOXALINECARBOXALDEHYDE,3-CHLORO

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:49568-68-5 SDS

49568-68-5Upstream product

49568-68-5Relevant articles and documents

Photoredox-Catalyzed Redox-Neutral Minisci C?H Formylation of N-Heteroarenes

Dong, Jianyang,Wang, Xiaochen,Song, Hongjian,Liu, Yuxiu,Wang, Qingmin

supporting information, p. 2155 - 2159 (2020/02/11)

We report a protocol for redox-neutral Minisci C?H formylation of N-heteroarenes using 1,3-dioxoisoindolin-2-yl 2,2-diethoxyacetate as a formyl equivalent at room temperature. This scalable benchtop protocol offers a distinct advantage over traditional reductive carbonylation and Minisci C?H formylation methods in not requiring the use of carbon monoxide, pressurized gas, a stoichiometric reductant, or a stoichiometric oxidant. (Figure presented.).

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