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3,4-diethyladiponitrile, also known as 3,4-diethylglutaronitrile, is an organic compound with the chemical formula C8H12N2. It is a colorless to pale yellow liquid with a characteristic odor. This chemical is primarily used as a monomer in the production of high-performance polymers, such as polyamide resins and fibers, due to its ability to form strong, heat-resistant materials. It is also employed as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. 3,4-diethyladiponitrile is known for its high reactivity and is often used in the preparation of other nitriles and amides. However, it is important to handle 3.4-diethyladiponitrile with care due to its potential toxicity and environmental impact.

4383-66-8

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4383-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4383-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4383-66:
(6*4)+(5*3)+(4*8)+(3*3)+(2*6)+(1*6)=98
98 % 10 = 8
So 4383-66-8 is a valid CAS Registry Number.

4383-66-8Downstream Products

4383-66-8Relevant academic research and scientific papers

Method for producing alcoxylated carbonyl compounds by an anodic oxidation method using a cathodic coupled reaction for organic synthesis

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Page column 5, (2008/06/13)

A method for producing alcoxylated carbonyl compounds of general formula (I) (compounds I): R1aR2C(OR3)bwherein R1, R2represent hydrogen or C1-C6-alkyl, R3independently means C1-C6-alkyl, a is 0 or 1, b 2 or 3 with the proviso that the sum of a and b is 3, by means of anodic oxidation of germinal dialcoxy compounds of general formula (II) (compounds II) wherein R4, R5, R6, R7represent hydrogen or C1-C6-alkyl, R5, R6represent C1-C6-alkyl or C1-C6-alcoxy, in the presence of a C1-C6-alkyl alcohol (compounds III). A usual compound (compound IV) is used as a cathodic depolarizer suitable for electrochemical oxidation. The anodic oxidation and cathodic reduction is carried out in an undivided electrolyte cell in the presence of C1-C6-alkyl alcohols.

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