878805-97-1

Basic information

• Product Name: 3-(methylsulfonyl)-2-Pyridinamine
• Synonyms: 3-(methylsulfonyl)-2-Pyridinamine;3-(Methylsulfonyl)pyridin-2-amine;2-PYRIDINAMINE, 3-(METHYLSULFONYL)-
• CAS NO: 878805-97-1
• Molecular Formula: C6H8N2O2S
• Molecular Weight: 172.20492
• EINECS: -0
• Mol File: 878805-97-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 405.4±45.0 °C(Predicted)
• Appearance: /
• Density: 1.358±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 2.92±0.36(Predicted)
• CAS DataBase Reference: 3-(methylsulfonyl)-2-Pyridinamine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(methylsulfonyl)-2-Pyridinamine(878805-97-1)
• EPA Substance Registry System: 3-(methylsulfonyl)-2-Pyridinamine(878805-97-1)

Safety Data

• Hazardous Substances Data: 878805-97-1(Hazardous Substances Data)

Usage

General Description

3-(methylsulfonyl)-2-Pyridinamine is a chemical compound with the molecular formula C7H9N3O2S. It is a pyridine derivative that contains a methylsulfonyl group attached to the third carbon atom of the pyridine ring. 3-(methylsulfonyl)-2-Pyridinamine has been studied for its potential applications in pharmaceuticals and agrochemicals due to its ability to inhibit certain enzymes and pathways. It is also used as a building block in the synthesis of other organic compounds. Additionally, 3-(methylsulfonyl)-2-pyridinamine has been investigated for its potential use as a corrosion inhibitor in industrial applications. Overall, this compound has diverse potential uses in various fields due to its unique chemical structure and properties.

Upstream product

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Relevant articles and documents

Synthesis method and applications of polysubstituted 2-aminopyridine derivative

The invention belongs to the field of organic synthetic chemistry, and relates to a synthetic method and applications of a polysubstituted 2-aminopyridine derivative. According to the method, a 1,2,3-triazine compound and a cyanomethyl compound are used as substrates and are subjected to a one-step cycloaddition reaction under an alkaline condition to obtain a polysubstituted 2-aminopyridine derivative, wherein the reaction does not involve in danger and control reagents and medicines, and a simple, safe, efficient and environment-friendly strategy is provided for synthesizing the polysubstituted 2-aminopyridine derivative. According to the present invention, the obtained product is subjected to further derivatization, such that the active molecule or the drug molecule containing the 2-aminopyridine structure can be synthesized, such as active molecule SC-53606, drug molecule apatinib and nevirapine.

INDOLIN-2-ONE DERIVATIVES USEFUL IN THE TREATMENT OF CNS DISEASES

The present invention is concerned with indolin-2-one derivatives of general formula (I) wherein A is phenyl or a six membered heteroaryl group, containing one or two N atoms, selected from (II) R1 is S(0)2lower alkyl, S(0)2NR4R

NOVEL SUBSTITUTED IMIDAZOLE DERIVATIVES

The present invention relates to a compound represented by Formula [I] or a pharmaceutically acceptable salt or ester thereof: wherein: X1, X2, X3, and X4, which may be identical or different, are each C or N, provided that none to two of X1, X2, X3, and X4 is/are N; Y is CH or N; R1, R1', R2, R2', R3, R3', R4, and R4', which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R5 is a hydrogen atom or a methyl group; R6 and R7, which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R8 and R8', which may be identical or different, are each a hydrogen atom, a lower alkyl group, or the like; R9 is an aryl group or a heteroaryl group which may be substituted; and n is an integer from 1 to 3, and a PLK1 inhibitor or an anticancer agent containing the same.