What is the 4-(3-Pyridyl)-2-chloropyrimidine?

4-(3-Pyridyl)-2-chloropyrimidine is , while it's Molecular Formula is C9H6ClN3. Used in Pharmaceutical Industry: 4-(3-Pyridyl)-2-chloropyrimidine is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of various drugs. Its unique functional groups allow for the development of biologically active compounds with potential therapeutic applications. Used in Agrochemical Industry: In the agrochemical industry, 4-(3-Pyridyl)-2-chloropyrimidine serves as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products. Used in Anticancer Research: 4-(3-Pyridyl)-2-chloropyrimidine is used as a potential anticancer agent in research, due to its ability to be modified and incorporated into compounds that target cancer cells. Its unique structure allows for the exploration of its potential in inhibiting the growth and proliferation of cancerous cells. Used in Antimicrobial Research: This chemical compound is also utilized in the development of antimicrobial agents, as its structure can be manipulated to target and combat various microorganisms, contributing to the discovery of new antibiotics and antifungal agents. Used in Medicinal Chemistry Research: 4-(3-Pyridyl)-2-chloropyrimidine is employed in medicinal chemistry research for its potential to be a key component in the synthesis of novel compounds with therapeutic properties. Its functional groups provide a foundation for further chemical modifications and exploration of its biological activity. Used in Organic Chemistry Research: In the field of organic chemistry, 4-(3-Pyridyl)-2-chloropyrimidine is used in various research applications, including the study of reaction mechanisms, synthesis techniques, and the development of new organic compounds with potential applications in various industries.

What is the CAS number for 4-(3-Pyridyl)-2-chloropyrimidine?

The CAS number of 4-(3-Pyridyl)-2-chloropyrimidine is 483324-01-2.

What is 4-(3-Pyridyl)-2-chloropyrimidine (483324-01-2) used for?

4-(3-Pyridyl)-2-chloropyrimidine, also known as 2-Chloro-4-(3-pyridyl)pyrimidine, is a pyrimidine derivative with the molecular formula C8H6ClN3. It features a chloro group and a pyridyl group as its functional groups, making it a versatile chemical compound used in various applications.InChI:InChI=1/C9H6ClN3/c10-9-12-5-3-8(13-9)7-2-1-4-11-6-7/h1-6H

What is the 4-(3-Pyridyl)-2-chloropyrimidine?

4-(3-Pyridyl)-2-chloropyrimidine is , while it's Molecular Formula is C9H6ClN3. Used in Pharmaceutical Industry: 4-(3-Pyridyl)-2-chloropyrimidine is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of various drugs. Its unique functional groups allow for the development of biologically active compounds with potential therapeutic applications. Used in Agrochemical Industry: In the agrochemical industry, 4-(3-Pyridyl)-2-chloropyrimidine serves as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products. Used in Anticancer Research: 4-(3-Pyridyl)-2-chloropyrimidine is used as a potential anticancer agent in research, due to its ability to be modified and incorporated into compounds that target cancer cells. Its unique structure allows for the exploration of its potential in inhibiting the growth and proliferation of cancerous cells. Used in Antimicrobial Research: This chemical compound is also utilized in the development of antimicrobial agents, as its structure can be manipulated to target and combat various microorganisms, contributing to the discovery of new antibiotics and antifungal agents. Used in Medicinal Chemistry Research: 4-(3-Pyridyl)-2-chloropyrimidine is employed in medicinal chemistry research for its potential to be a key component in the synthesis of novel compounds with therapeutic properties. Its functional groups provide a foundation for further chemical modifications and exploration of its biological activity. Used in Organic Chemistry Research: In the field of organic chemistry, 4-(3-Pyridyl)-2-chloropyrimidine is used in various research applications, including the study of reaction mechanisms, synthesis techniques, and the development of new organic compounds with potential applications in various industries.

What is the CAS number for 4-(3-Pyridyl)-2-chloropyrimidine?

The CAS number of 4-(3-Pyridyl)-2-chloropyrimidine is 483324-01-2.

What is 4-(3-Pyridyl)-2-chloropyrimidine (483324-01-2) used for?

4-(3-Pyridyl)-2-chloropyrimidine, also known as 2-Chloro-4-(3-pyridyl)pyrimidine, is a pyrimidine derivative with the molecular formula C8H6ClN3. It features a chloro group and a pyridyl group as its functional groups, making it a versatile chemical compound used in various applications.InChI:InChI=1/C9H6ClN3/c10-9-12-5-3-8(13-9)7-2-1-4-11-6-7/h1-6H

Manufacturer supply 4-(3-Pyridyl)-2-chloropyrimidine 483324-01-2 with sufficient stock and high standard

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Product

4-(3-Pyridyl)-2-chloropyrimidine

CAS No.: 483324-01-2

product details:

Purity: 99%

Manufacturer supply 4-(3-Pyridyl)-2-chloropyrimidine 483324-01-2 with sufficient stock and high standard

Molecular Formula: C9H6ClN3
Molecular Weight: 191.62
Vapor Pressure: 3.14E-06mmHg at 25°C
Refractive Index: 1.599
Boiling Point: 399.5 °C at 760 mmHg
PKA: 2.34±0.12(Predicted)
Flash Point: 227.7 °C
PSA： 38.67000
Density: 1.309 g/cm³
LogP: 2.19200

4-(3-Pyridyl)-2-chloropyrimidine(Cas 483324-01-2) Usage

General Description

4-(3-Pyridyl)-2-chloropyrimidine, also known as 2-Chloro-4-(3-pyridyl)pyrimidine, is a chemical compound with the molecular formula C8H6ClN3. It is a pyrimidine derivative that contains a chloro group and a pyridyl group as its functional groups. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also employed in the development of biologically active compounds, including potential anticancer and antimicrobial agents. Additionally, 4-(3-Pyridyl)-2-chloropyrimidine may be utilized in various research applications in the fields of medicinal and organic chemistry.

InChI:InChI=1/C9H6ClN3/c10-9-12-5-3-8(13-9)7-2-1-4-11-6-7/h1-6H

483324-01-2 Relevant articles

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483324-01-2 Process route

: 3934-20-1
2,6-Dichloropyrimidine

: 1692-25-7
3-pyridylboronic acid

: 483324-01-2
2-chloro-4-(pyridin-3-yl)pyrimidine

Conditions

Conditions	Yield
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; caesium carbonate; In tetrahydrofuran; water; at 85 ℃; for 12h; Inert atmosphere;	81%
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In 1,4-dioxane; water; at 90 ℃; for 4h; Reagent/catalyst; Temperature; Inert atmosphere; Green chemistry;	74.6%
With sodium carbonate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; water; for 16h; Heating; Reflux; Inert atmosphere;	73%
With bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; for 14h; Reflux; Inert atmosphere;	52%
With sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; water; at 60 ℃; for 16h;
With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In 1,2-dimethoxyethane; water; at 100 ℃; for 1h;
With bis-triphenylphosphine-palladium(II) chloride; triethylamine; at 80 ℃;

: 626-55-1,163928-56-1
3-Bromopyridine

: 1722-12-9,1195939-87-7
2-chloropyrimidine

: 483324-01-2
2-chloro-4-(pyridin-3-yl)pyrimidine

Conditions

Conditions	Yield
3-Bromopyridine; 2-chloropyrimidine; With n-butyllithium; In diethyl ether; hexane; at -30 - 0 ℃; for 1.5h; With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; diethyl ether; hexane; at 23 ℃; for 0.25h;	94%
3-Bromopyridine; With n-butyllithium; In diethyl ether; hexane; at -78 ℃; for 1h; Inert atmosphere; 2-chloropyrimidine; In diethyl ether; hexane; at -30 - 0 ℃; for 1.66667h; With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; diethyl ether; hexane; water; at 0 - 20 ℃; for 0.25h;	53%