91973-39-6

Basic information

• Product Name: (2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE
• Synonyms: (2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE;METHANONE, (2-AMINOPHENYL)-4-PYRIDINYL-
• CAS NO: 91973-39-6
• Molecular Formula: C₁₂H₁₀N₂O
• Molecular Weight: 198.22
• Mol File: 91973-39-6.mol
• Article Data: 16

Chemical Properties

• Melting Point: 160-161 °C
• Boiling Point: 412.9±25.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C(protect from light)
• PKA: 2.66±0.10(Predicted)
• CAS DataBase Reference: (2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE(91973-39-6)
• EPA Substance Registry System: (2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE(91973-39-6)

Safety Data

• Hazardous Substances Data: 91973-39-6(Hazardous Substances Data)

Usage

General Description

(2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE is a chemical compound with the molecular formula C12H10N2O. It consists of a pyridine ring with a phenyl group and an amino group attached to it, as well as a carbonyl group at the 4-position of the pyridine ring. (2-AMINO-PHENYL)-PYRIDIN-4-YL-METHANONE is commonly used in organic synthesis and pharmaceutical research due to its versatile reactivity and potential pharmacological properties. It may possess biological activities such as anticancer, antimicrobial, and anti-inflammatory properties, making it a valuable target for drug development and medicinal chemistry studies.

Upstream product

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• 78500-74-0 (2-nitrophenyl)(pyridin-4-yl)methanol 
• 6625-74-7 N-pivaloylaniline 
• 126971-79-7 N-{2-[hydroxy(pyridin-4-yl)methyl]-phenyl}-2,2-dimethylpropanamide 

Downstream Products

• 115177-78-1 1-(2-amino-phenyl)-1-[4]pyridyl-ethanol 
• 18631-22-6 5H-indeno[1,2-c]pyridin-5-one 
• 827575-89-3 N-(4-{[(2-isonicotinoylphenyl)amino]sulfonyl}phenyl)acetamide 
• 1224437-09-5 C₂₂H₂₅N₃O₄ 
• 115177-74-7 <1-2H>-1-(2-azidophenyl)-1-(4-pyridyl)ethane 
• 115177-73-6 C₁₃H₁₃⁽²⁾HN₂ 
• 115177-72-5 1-(2-aminophenyl)-1-(4-pyridyl)ethane 
• 115177-75-8 2-(1-Pyridin-4-yl-vinyl)-phenylamine 
• 153404-03-6 (1-Methyl-2-oxo-5-pyridin-4-yl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-carbamic acid benzyl ester 
• 1055963-39-7 {Amino-[2-(pyridine-4-carbonyl)-phenylcarbamoyl]-methyl}-carbamic acid benzyl ester 
• 154064-09-2 [2-Oxo-1-(2-oxo-2-o-tolyl-ethyl)-5-pyridin-4-yl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl]-carbamic acid benzyl ester 
• 152665-86-6 [1-(2-Cyclopentyl-2-oxo-ethyl)-2-oxo-5-pyridin-4-yl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl]-carbamic acid benzyl ester 

Relevant articles and documents

PYRIDINIUM DERIVATIVES AS HERBICIDES

Compounds of the formula (I) (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially as herbicides.

With anti-tumor activity of triazole b the nitrogen is outstanding compound and its preparation method (by machine translation)

The invention discloses a with anti-tumor activity of triazole b the nitrogen is outstanding compound and its preparation method, which belongs to the technical field of medical synthesis. Technical point of the invention is: The invention compared with the prior art has the following advantages: the invention synthetic method is simple, novel and molecular structure can be integrated two nitrogen test paper compound and the triazole compound of the advantages of biological activity, to the breast cancer cell MCF - 7 and liver cancer cell HepG2 inhibition, is expected to be in the direction of the anti-tumor drugs further popularization and application. (by machine translation)

A novel benzodiazepine three-ring compound and its preparation method and application (by machine translation)

The invention discloses a novel benzodiazepine three-ring compound and its preparation method and application, which belongs to the technical field of medical synthesis. Technical proposal of the invention points are: a novel benzodiazepine three-ring compound, has the following structure: Wherein R is O or S. The invention also discloses a novel benzodiazepine tricyclic compound of the preparation method. The invention a new method to synthesize a novel benzodiazepine three-ring compound, the reaction process is simple and easy operation, the raw material is cheap, environmental protection, higher reaction efficiency and good repeatability, has good anti-platelet aggregation activity and anti-tumor activity. (by machine translation)