15519-86-5 Usage
Description
MALEIC ACID MONO ETHANOLAMIDE, also known as N-(2-Hydroxyethyl)maleamic Acid, is an organic compound with the CAS number 15519-86-5. It is characterized by its sticky, waxy solid appearance and is primarily used in organic synthesis due to its unique chemical properties.
Uses
Used in Organic Synthesis:
MALEIC ACID MONO ETHANOLAMIDE is used as a synthetic building block for the creation of various organic compounds. Its chemical structure allows it to be a versatile component in the synthesis of different molecules, contributing to the development of new materials and chemicals.
Used in Pharmaceutical Industry:
MALEIC ACID MONO ETHANOLAMIDE is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique properties make it a valuable component in the development of new drugs, potentially leading to the creation of novel medications with improved efficacy and reduced side effects.
Used in Chemical Industry:
In the chemical industry, MALEIC ACID MONO ETHANOLAMIDE is used as a raw material for the production of various chemicals and materials. Its sticky, waxy solid nature makes it suitable for use in the formulation of products such as adhesives, coatings, and other industrial applications.
Used in Research and Development:
MALEIC ACID MONO ETHANOLAMIDE is also utilized in research and development settings, where it serves as a key compound in the exploration of new chemical reactions and the discovery of novel synthetic pathways. Its unique properties make it an essential tool for chemists and researchers working on the cutting edge of chemical innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 15519-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,1 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15519-86:
(7*1)+(6*5)+(5*5)+(4*1)+(3*9)+(2*8)+(1*6)=115
115 % 10 = 5
So 15519-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO4/c8-4-3-7-5(9)1-2-6(10)11/h1-2,8H,3-4H2,(H,7,9)(H,10,11)/b2-1-
15519-86-5Relevant articles and documents
Functionalized olefin polymers, compositions and articles prepared therefrom, and methods for making the same
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Page/Page column 73, (2015/12/17)
In one aspect the invention provides a melt process for preparing a functionalized olefin multiblock interpolymer, said process comprising grafting onto the backbone of the olefin multiblock interpolymer at least one compound comprising at least one “amine-reactive” group to form a grafted olefin multiblock interpolymer, and reacting a primary-secondary diamine or an alkanolamine with the grafted olefin multiblock interpolymer, without the isolation of the grated olefin multiblock interpolymer.
Synthesis of New Bifunctional Maleimide Compounds for the Preparation of Chemoimmunoconjugates
Beyer,Krüger,Schumacher,Unger,Kratz
, p. 91 - 102 (2007/10/03)
Bifunctional maleimide compounds are suitable for binding small molecules to carrier proteins in that they bind to the sulfhydryl group of proteins through the double bond of the maleimide group and to molecules of low molecular weight (e.g. anticancer drugs) through a functional group X. 18 maleimide compounds of the general formula Maleimid-R-X (R = phenylene, benzyl-, methylene-, ethylene, or a m-benzoylethylamide group and X = hydroxy-, amino-, hydrazino-, carboxylic acid-, carboxylic anhydride-, carboxylic acid chloride-, carboxylic acid hydrazide-, oxycarbonylchloride-, aldehyde, keto-, or p-toluenesulfonate-group) were synthesized and characterized through 1H- and 13C-NMR-spectroscopy, elemental analysis, and mass spectrometry.
