105-93-1 Usage
Uses
Used in Chemical Synthesis:
1,2-Ethanediamine,N1,N2-diethyl-N1-[2-(ethylamino)ethyl]is used as a chemical intermediate for the synthesis of various compounds in the chemical industry. Its unique structure and reactivity make it a valuable building block for the development of new materials and products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,2-Ethanediamine,N1,N2-diethyl-N1-[2-(ethylamino)ethyl]is used as a precursor for the development of new drugs. Its chemical properties may allow for the creation of novel therapeutic agents with unique mechanisms of action.
Used in Research and Development:
1,2-Ethanediamine,N1,N2-diethyl-N1-[2-(ethylamino)ethyl]is utilized in research and development settings to study its chemical properties and potential applications. Scientists and researchers can use 1,2-Ethanediamine,N1,N2-diethyl-N1-[2-(ethylamino)ethyl]- to explore its reactivity, stability, and interactions with other molecules, which may lead to new discoveries and innovations.
Used in Material Science:
In the field of material science, 1,2-Ethanediamine,N1,N2-diethyl-N1-[2-(ethylamino)ethyl]may be used to develop new materials with specific properties. Its unique structure could contribute to the creation of advanced materials with applications in various industries, such as electronics, aerospace, or automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 105-93-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105-93:
(5*1)+(4*0)+(3*5)+(2*9)+(1*3)=41
41 % 10 = 1
So 105-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H25N3/c1-4-11-7-9-13(6-3)10-8-12-5-2/h11-12H,4-10H2,1-3H3
105-93-1Relevant academic research and scientific papers
Reaction of 1,2-dibromoethane with primary amines: Formation of N,N′-disubstituted ethylenediamines RNH-CH2CH2-NHR and homologous polyamines RNH-[CH2CH2NR]n-H
Denk, Michael K.,Krause, Mike J.,Niyogi, Debyani F.,Gill, Nachhattarpal K.
, p. 7565 - 7570 (2007/10/03)
The reaction of primary amines RNH2 (R: Me, Et, iPr, tBu and Ph) with 1,2-dibromoethane gave N,N′-disubstituted ethylenediamines R-NH-CH2CH2-NH-R (1) in yields ranging from 10% (1a; R=Me) to 70% (1d, R=tBu; 1e, R=Ph). Pipe
ALKYLATION OF ACYCLIC AND CYCLIC DIAMINES AND POLYAMINES
Zagudullin, R. N.,Baimetov, Z. M.
, p. 889 - 894 (2007/10/02)
Alkylation of diamines and polyamines by allyl and methallyl chlorides or by chloropropenes has been used to obtain polyalkylpolyamines that had not been described previously.The alkylation of the polyamines by allyl and methallyl chlorides proceeds more energetically in comparison with the alkylation by ethyl chloride or chloropropenes.The alkylation of either cyclic and acyclic polyamines begins with the primary amino group.With increasing length of the chain and the alkyl radical at the nitrogen of the alkylated polyamines, their capability for reacting with the evolved hydrogen chloride drops off, and this leads to a decrease in yield of the desired products owing to the loss of activity of the original or partly alkylated polyamines.
