100396-39-2 Usage
Uses
Used in Solvent Applications:
BIS(2-PYRROLIDINOETHYL) ETHER is used as a solvent in various industries for its ability to dissolve a wide range of substances. It is particularly useful in applications such as inks, dyes, adhesives, and coatings, where its solubility properties enhance the performance and functionality of these products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, BIS(2-PYRROLIDINOETHYL) ETHER is utilized as a coupling agent and emulsifier. Its role in these processes is crucial for the production of various pharmaceuticals and personal care products, where it helps to improve the stability, consistency, and effectiveness of the final products.
Used in Personal Care Products:
Similarly, in the personal care sector, BIS(2-PYRROLIDINOETHYL) ETHER contributes to the formulation of products by acting as a coupling agent and emulsifier. This enhances the texture, spreadability, and overall performance of personal care products, ensuring they meet consumer expectations for quality and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 100396-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,9 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100396-39:
(8*1)+(7*0)+(6*0)+(5*3)+(4*9)+(3*6)+(2*3)+(1*9)=92
92 % 10 = 2
So 100396-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H24N2O/c1-2-6-13(5-1)9-11-15-12-10-14-7-3-4-8-14/h1-12H2
100396-39-2Relevant academic research and scientific papers
METHOD FOR PRODUCING BISPYRROLIDINE COMPOUNDS
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Paragraph 0057; 0059-0062, (2020/12/25)
The present application relates to a method for preparing compounds of the formula I in which, in a first step, γ-butyrolactone is reacted with diamines of the formula II to form bisamides of the formula III, with the amide function of the bisamides of the formula III then undergoing partial or complete catalytic hydrogenation in step II) to form bispyrrolidine compounds of the formula I.
