612-11-3

Basic information

• Product Name: 3,4-DIETHYL PYRIDINE
• Synonyms: 3,4-DIETHYL PYRIDINE
• CAS NO: 612-11-3
• Molecular Formula: C₉H₁₃N
• Molecular Weight: 135.21
• EINECS: 210-290-2
• Mol File: 612-11-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 205.5°C at 760 mmHg
• Flash Point: 74.6°C
• Appearance: /
• Density: 0.911g/cm³
• Vapor Pressure: 0.357mmHg at 25°C
• Refractive Index: 1.497
• CAS DataBase Reference: 3,4-DIETHYL PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIETHYL PYRIDINE(612-11-3)
• EPA Substance Registry System: 3,4-DIETHYL PYRIDINE(612-11-3)

Safety Data

• Hazardous Substances Data: 612-11-3(Hazardous Substances Data)

Usage

General Description

3,4-Diethyl pyridine is a chemical compound consisting of a pyridine ring with two ethyl groups attached at positions 3 and 4. It is a colorless liquid with a strong, unpleasant odor. 3,4-Diethyl pyridine is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. It is also used as a building block in the production of agrochemicals and insecticides. Additionally, 3,4-Diethyl pyridine is utilized in the manufacturing of rubber chemicals and antioxidants. Due to its chemical properties and applications, it is important to handle this substance with care and follow proper safety protocols when working with it.

InChI:InChI=1/C9H13N/c1-3-8-5-6-10-7-9(8)4-2/h5-7H,3-4H2,1-2H3

Upstream product

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Downstream Products

• 60333-19-9 1,2-dibenzyl-3,4-diethyl-1,2,5,6-tetrahydropyridine 
• 129254-94-0 1-phenyl-3-(3-ethyl-pyridin-4-yl)-butane 

Relevant articles and documents

Inhibitors of cell proliferation, angiogenesis, fertility, and muscle contraction

The invention concerns inhibitors of cell proliferation, angiogenesis, fertility, and muscle contraction, characterized by formula I wherein, X, Y and Z independently represent C or N; ------ is an optional double bond; n is 0 or 1; R1, R2, and R4 independently represent hydrogen, a chemical bond, C1-10 alkyl; C2-10 alkenyl; C2-10 alkinyl; aryl; aryl-C1-10 alkyl; C3-10 heterocyclyl; C5-10 heteroaryl; halo, CF3; NO2; NHC(O)R*, OR, said alkyl, alkenyl, alkinyl, aryl, arylalkyl, heterocyclyl, or heteroaryl being optionally substituted; R3, R5, and R6 independently represent hydrogen, C1-10alkyl; C2-10 alkenyl; C2-10 alkinyl; aryl; aryl-C1-10alkyl; C3-10 heterocyclyl; C5-10 heteroaryl; halo, CF3; NO2; NHC(O)R*, OR, said alkyl, alkenyl, alkinyl, aryl, heterocyclyl, or heteroaryl being optionally substituted; or R5 and R6 together form a 5- or 6-member aryl, heterocyclyl or heteroaryl group; R is hydrogen or C1-6 alkyl; R* is hydrogen, or C1-6 alkyl, or OH, wherein the optional substituents are preferably selected from the group of one to three OH, C1-6 alkyl, halo, NO2, C1-6 alkoxy, and CF3, or a pharmaceutically acceptable salt thereof.