612-11-3 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Diethyl pyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Dye Industry:
In the dye industry, 3,4-diethyl pyridine is utilized as a building block for the production of dyes, contributing to the creation of a diverse range of colorants for different applications.
Used in Agrochemical Industry:
3,4-Diethyl pyridine is employed as a precursor in the production of agrochemicals, particularly insecticides, where its chemical structure plays a crucial role in the effectiveness of these products.
Used in Rubber Chemical Industry:
3,4-DIETHYL PYRIDINE is used as a component in the manufacturing of rubber chemicals, enhancing the properties of rubber products and contributing to their performance and durability.
Used in Antioxidant Production:
3,4-Diethyl pyridine is also utilized in the production of antioxidants, which are essential in preventing the oxidation of materials, thereby extending their shelf life and improving their stability.
Given the wide range of applications and the chemical properties of 3,4-diethyl pyridine, it is imperative to handle this substance with care and adhere to proper safety protocols to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 612-11-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 612-11:
(5*6)+(4*1)+(3*2)+(2*1)+(1*1)=43
43 % 10 = 3
So 612-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N/c1-3-8-5-6-10-7-9(8)4-2/h5-7H,3-4H2,1-2H3
612-11-3Relevant academic research and scientific papers
Inhibitors of cell proliferation, angiogenesis, fertility, and muscle contraction
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, (2008/06/13)
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.
