142-25-6 Usage
Description
N,N,N'-Trimethylethylenediamine, also known as N,N,N'-trimethyl-1,2-ethanediamine, is an organic compound with the chemical formula (CH3)3NCH2CH2NH2. It is a clear colorless liquid synthesized using laser-vaporization supersonic molecular beam and has been studied using pulsed-field ionization zero electron kinetic energy. N,N,N'-TRIMETHYLETHYLENEDIAMINE is characterized by its amine functional groups and is known for its versatile applications in various industries.
Uses
Used in Surfactant Synthesis:
N,N,N'-Trimethylethylenediamine is used as a precursor in the synthesis of a novel gemini surfactant, specifically N,N-dimethyl-N-2-[N'-methyl-N'-(3-sulfopropyl)-alkylammonium]ethyl-1-alkylammonium bromides. These gemini surfactants are known for their enhanced properties compared to traditional surfactants, such as better solubility, lower critical micelle concentration, and improved surface activity.
Used in Pharmaceutical Industry:
N,N,N'-Trimethylethylenediamine is used as an amine component for in-situ formation of alpha-amino alkoxides, which are important intermediates in the synthesis of various pharmaceutical compounds. The compound's reactivity and amine functionality make it a valuable building block for the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
The compound is involved in the synthesis of N,N'-dimethyl-N'-(2-hydroxy-aethyl)-aethylendiamin, which is an important organic compound with various applications in the chemical industry. N,N,N'-Trimethylethylenediamine's versatility as a synthetic building block allows it to be used in the production of a wide range of chemicals, including those used in the manufacturing of dyes, pigments, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 142-25-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 142-25:
(5*1)+(4*4)+(3*2)+(2*2)+(1*5)=36
36 % 10 = 6
So 142-25-6 is a valid CAS Registry Number.
142-25-6Relevant articles and documents
Multi-ammonia dithio-formic acid sulfite derivative and preparation method and application thereof
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Paragraph 0111-0118, (2017/07/07)
The invention provides a multi-ammonia dithio-formic acid sulfite derivative which has a structure as shown in a formula (I). The invention further provides a method for preparing the derivative and application of the derivative as a reducing agent - chain transfer agent to the aspect of free radical polymerization reaction. A preparation method is simple, reaction conditions are mild, and the multi-ammonia dithio-formic acid sulfite derivative has very good application effects and application values in the free radical polymerization reaction triggered in an oxidation-reduction system.
METHOD FOR PRODUCING N-MONOALKYL-SUBSTITUTED ALKYLENE AMINE
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Page/Page column 8, (2010/02/11)
PROBLEM TO BE SOLVED: To provide a method for producing an N-monoalkyl-substituted alkylene amine especially useful for uses such as medicine intermediates, agrochemical intermediates, urethane resin-foaming catalysts, surfactants and the like among alkyl-substituted alkylene amine compounds from an alcohol and an alkylene amine as raw materials. SOLUTION: This method for producing the N-monoalkyl-substituted alkylene amine is characterized by reacting the alkylene amine with a ≥2C alkyl alcohol in the presence of a copper-containing oxide catalyst system. The N-monoalkyl-substituted alkylenamine is produced in high conversion and in N-monoalkylation selectivity.
Tetracyclic benzimidazole derivatives and combinatorial libraries thereof
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, (2008/06/13)
The present invention relates to novel tetracyclic benzimidazole derivative compounds of the following formula: wherein R1to R10have the meanings described in here. The invention further relates to combinatorial libraries containing two or more such compounds, as well as methods of preparing tetracyclic benzimidazole derivative compounds.