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59715-45-6

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59715-45-6 Usage

Description

5,6-Dichloropyrazine-2,3-dicarboxylic acid is a white crystalline chemical compound belonging to the pyrazine-2,3-dicarboxylic acid family. It has a molecular formula of C6H2Cl2N2O4 and a molecular weight of 228.995 g/mol. 5,6-Dichloropyrazine-2,3-dicarboxylic acid is soluble in water and has a melting point of 270-275°C. It is recognized for its potential as a building block in the synthesis of pharmaceutical and agrochemical compounds, as well as for its antioxidant and radical scavenging properties, which make it a promising candidate for research in medicine and biotechnology.

Uses

Used in Pharmaceutical Industry:
5,6-Dichloropyrazine-2,3-dicarboxylic acid is used as a key building block for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5,6-Dichloropyrazine-2,3-dicarboxylic acid serves as a crucial intermediate in the production of agrochemicals. Its incorporation into these compounds can enhance their effectiveness in agricultural applications.
Used in Antioxidant Research:
5,6-Dichloropyrazine-2,3-dicarboxylic acid is used as a subject of research in antioxidant applications due to its potential antioxidant and radical scavenging properties. These properties could lead to the development of new antioxidants for use in medicine and biotechnology.
Used in Biotechnology Research:
5,6-Dichloropyrazine-2,3-dicarboxylic acid is also utilized in biotechnology research to explore its potential applications in various biological systems. Its unique structure and properties may contribute to advancements in biotechnological processes and products.

Check Digit Verification of cas no

The CAS Registry Mumber 59715-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,1 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59715-45:
(7*5)+(6*9)+(5*7)+(4*1)+(3*5)+(2*4)+(1*5)=156
156 % 10 = 6
So 59715-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl2N2O4/c7-3-4(8)10-2(6(13)14)1(9-3)5(11)12/h(H,11,12)(H,13,14)

59715-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Dichloropyrazine-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 5,6-dichloro-pyrazine-2,3-dicarboxylic acid

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:59715-45-6 SDS

59715-45-6Relevant articles and documents

Bioorthogonal Ligation and Cleavage by Reactions of Chloroquinoxalines with ortho-Dithiophenols

Fu, Hua,Li, Hongyun,Li, Youshan,Lou, Zhenbang,Yang, Haijun,Zhao, Yufen

supporting information, p. 3671 - 3677 (2020/02/04)

A bioorthogonal ligation and cleavage method via reactions of chloroquinoxalines (CQ) and ortho-dithiophenols (DT) is presented. Double nucleophilic substitutions of ortho-dithiophenols to chloroquinoxalines provide conjugates containing tetracyclic benzo[5,6][1,4]dithiino[2,3-b]quinoxaline with strong built-in fluorescence together with release of the other functional molecules. Three cleavable linkers were designed and successfully used in release of the molecules containing biotin from the protein conjugates. The CQ-DT bioorthogonal reactions can be applied for the bioorthogonal ligations, bioorthogonal cleavages, and trans-tagging of proteins, and show advantages of readily accessible unnatural orthogonal groups, appealing reaction kinetics (k2≈1.3 m?1 s?1), excellent biocompatibility of orthogonal groups, and high stability of conjugates. This complements previous bioorthogonal reactions and is a new route for protein-fishing applications and in-gel fluorescence analysis.

Resorcinarene-based cavitands with chiral amino acid substituents for chiral amine recognition

Li, Na,Yang, Fan,Stock, Hillary A.,Dearden, David V.,Lamb, John D.,Harrison, Roger G.

scheme or table, p. 7392 - 7401 (2012/10/08)

Resorcinarene-based deep cavitands alanine methyl resorcinarene acid (AMA), alanine undecyl resorcinarene acid (AUA) and glycine undecyl resorcinarene acid (GUA), which contain chiral amino acids, have been synthesized. The upper rim of the resorcinarene host is elongated with four identical substituents topped with alanine and glycine groups. The structures of the new resorcinarenes were elucidated by nuclear magnetic resonance (NMR), mass spectrometry (MS) and the sustained off-resonance irradiation collision induced dissociation (SORI-CID) technique in FTICR-MS. These studies revealed that eight water molecules associate to the cavitand, two for each alanine group. The alanine substituent groups are proposed to form a kite-like structure around the resorcinarene scaffold. The binding of AMA, AUA, and GUA with chiral R- and S-methyl benzyl amines was studied by 1H NMR titration, and compared to that of a binary l-tartaric acid and the monoacid phthalyl alanine (PA). The results show that these compounds interact with amine guests; however, with four carboxylic acid groups, they bind several amine molecules strongly while the binary l-tartaric acid only binds one amine guest strongly. The simple compound PA, which contains one carboxylic group, shows weak binding to the amines. The 1H NMR titration of AUA with primary, secondary, and tertiary chiral amines showed that it can discriminate between these three types of amines and showed chiral discrimination for chiral secondary amines.

Permanganate Oxidation of Quinoxaline and Its Derivatives

Obafemi, Craig A.,Pfleiderer, Wolfgang

, p. 1549 - 1556 (2007/10/02)

The oxidation reaction of a series of quinoxaline derivatives, using KMnO4 in the presence or absence of NaOH, are described.Neutral oxidation of 2-chloro- and 2,3-dichlorodioxalines 2-4 afforded the corresponding chloro- and dichloropyrazinedicarboxilic acids 13 and 14 in good yield.On the other hand, oxidation of quinoxalin-2(1H)-one and 1,4-dihydroquinoxaline-2,3-dione derivatives in alkaline medium gave different products, with the quinoxalin-2(1H)-one (5) forming 1,4-dihydroquinoxaline-2,3-dione (9), while various substituted quinoxalin-2,3-dione derivatives (see 9-11) gave a new type of dimeric products.The structural assignments for the new compounds were based on spectroscopic data.

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