cas 3177-24-0|| where to buy 2,4-dichloropyrimidine-5-carbonitrile

Produktname:2,4-dichloropyrimidine-5-carbonitrile

IUPAC Name:2,4-dichloropyrimidine-5-carbonitrile

: CAS：3177-24-0; Molekulare Formel：C5HCl2N3; Reinheit：97%

: Katalognummer：CM107765; Molekulargewicht：173.98

Packungseinheit	Verfügbarer Vorrat	Preis($)
CM107765-10g	in stock	ŽƩ
CM107765-25g	in stock	Ĝřř

Anfrage: sales@chemenu.com

Nur für den Einsatz in Forschung und Entwicklung..

Anfrage-Formular

Chemische Bezeichnung

CAS-Nummer

Menge*

Erforderliche Spezifikationen*
(Gehalt %, Materialqualität etc.)

Name des Ansprechpartners*

E-Mail des Ansprechpartners*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 3177-24-0 regularly via the above email.

Zusätzliche Hinweise

Verification code*

refresh

Produkt-Details

: CAS-Nr.:3177-24-0; Molekulare Formel:C5HCl2N3; Schmelzpunkt:-; SMILES-Code:N#CC1=CN=C(Cl)N=C1Cl; Dichte:

: Katalognummer:CM107765; Molekulargewicht:173.98; Siedepunkt:; Mdl-Nr.:MFCD09746248; Lagerung:

Category Infos

: Pyrimidines; Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.

Column Infos

: Pyrimidines

Product Other Information

Product Overview	2,4-Dichloropyrimidine-5-carbonitrile (DCPC) is a synthetic compound that has been widely studied in the scientific community due to its potential applications in scientific research and laboratory experiments.
Synthesis Method	2,4-Dichloropyrimidine-5-carbonitrile is synthesized through a multi-step process that involves the reaction of 2,4-dichloro-5-nitropyrimidine and potassium carbonate in aqueous solution. This reaction is followed by a hydrolysis reaction of the product with hydrochloric acid, which yields 2,4-Dichloropyrimidine-5-carbonitrile as the final product.
Chemical Properties	It is relatively easy to synthesize and it is widely available. Additionally, it is a relatively inexpensive compound, making it an attractive option for laboratory experiments. However, there are a few drawbacks to using 2,4-Dichloropyrimidine-5-carbonitrile in laboratory experiments. For example, it is a relatively unstable compound, making it difficult to store for extended periods of time. Additionally, it has a relatively short half-life, meaning that it must be used quickly after it is synthesized.
Synthesis and Application	2,4-Dichloropyrimidine-5-carbonitrile has been widely used in scientific research due to its ability to act as an inhibitor of enzymes, such as cytochrome P450 (CYP) and cytochrome b5 (CYB5). It also acts as an inhibitor of the enzyme, cytochrome c oxidase, which is involved in the production of cellular energy. Additionally, 2,4-Dichloropyrimidine-5-carbonitrile has been used in the study of the metabolism of drugs and other compounds, as well as in the study of the regulation of gene expression.
Future Directions	One possible direction is to further explore its potential use as an inhibitor of enzymes, such as CYP and CYB5. Additionally, further research could be conducted to explore its potential use in the study of the metabolism of drugs and other compounds, as well as in the study of the regulation of gene expression. Additionally, research could be conducted to improve the stability and shelf-life of the compound, as well as to further investigate its biochemical and physiological effects. Finally, research could be conducted to explore other potential applications of 2,4-Dichloropyrimidine-5-carbonitrile in scientific research and laboratory experiments.