216076-11-8

Basic information

• Product Name: 1-(2-CHLORO-PHENYL)-2-PYRIDIN-4-YL-ETHANONE
• Synonyms: 1-(2-CHLORO-PHENYL)-2-PYRIDIN-4-YL-ETHANONE;1-(2-chlorophenyl)-2-(4-pyridinyl)Ethanone
• CAS NO: 216076-11-8
• Molecular Formula: C₁₃H₁₀ClNO
• Molecular Weight: 231.68
• Mol File: 216076-11-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 357 °C at 760 mmHg
• Flash Point: 169.7 °C
• Appearance: /
• Density: 1.239 g/cm³
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 1-(2-CHLORO-PHENYL)-2-PYRIDIN-4-YL-ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-CHLORO-PHENYL)-2-PYRIDIN-4-YL-ETHANONE(216076-11-8)
• EPA Substance Registry System: 1-(2-CHLORO-PHENYL)-2-PYRIDIN-4-YL-ETHANONE(216076-11-8)

Safety Data

• Hazardous Substances Data: 216076-11-8(Hazardous Substances Data)

Usage

General Description

1-(2-Chloro-phenyl)-2-pyridin-4-yl-ethanone is a chemical compound with a molecular formula C14H10ClNO. It is an organic compound that consists of a benzene ring with a chlorine atom attached at the 2-position, and a pyridine ring attached at the 4-position to an ethanone group. 1-(2-CHLORO-PHENYL)-2-PYRIDIN-4-YL-ETHANONE is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical products. It may also have potential applications in the field of organic synthesis and medicinal chemistry. The compound is a yellow or brown solid with a characteristic odor, and it is important to handle it with appropriate safety precautions due to its potential hazardous properties.

Upstream product

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Downstream Products

• 1311460-00-0 C₁₄H₁₃ClN₂O 
• 224038-78-2 [4-(2-chlorophenyl)-5-(4-pyridyl)-1,3-thiazol-2-yl]amine 

Relevant articles and documents

SELECTIVE SUBTYPE ALPHA 2 ADRENERGIC AGENTS AND METHODS FOR USE THEREOF

The invention provides well-defined heterocyclic compounds that are useful as subtype selective alpha 2 adrenergic agonists. As such, the compounds described herein are useful in treating a wide variety of disorders associated with selective subtype modulation of alpha 2 adrenergic receptors.

Synthesis and biological activities of 4-phenyl-5-pyridyl-1,3-thiazole derivatives as selective adenosine A3 antagonists

To investigate the potency of an adenosine A3 receptor (A 3AR) antagonist as an anti-asthmatic drug, a novel series of 4-phenyl-5-pyridyl-1,3-thiazole derivatives was synthesized and evaluated in human adenosine A1, A

MEDICINAL COMPOSITIONS

The present invention relates to an agent for the prophylaxis or treatment of pain, an agent for suppressing activation of osteoclast, and an inhibitor of osteoclast formation, which contains a p38 MAP kinase inhibitor and/or a TNF-α production inhibitor.