92074-11-8 Usage
Derivative of Ethylenediamine
Yes
It is derived from ethylenediamine, which is a basic building block in the formation of this compound.
Propyl Group Substitution
Methyldiphenylsilyl
The propyl group in the compound is substituted with a methyldiphenylsilyl group, which influences its chemical properties and reactivity.
Common Use
Ligand in chemical reactions
It is frequently used as a ligand, which helps in stabilizing and forming complexes with metal ions in various chemical reactions.
Building Block
Synthesis of complex organic compounds
The compound serves as a building block for the synthesis of more complex organic compounds, contributing to its versatility in chemical applications.
Crosslinking Agent
Production of polymers and resins
It is utilized as a crosslinking agent, which helps in the formation of polymers and resins with enhanced properties.
Chelating Agent
Metal ion coordination chemistry
Industrial Applications
Chemistry, materials science, and manufacturing
It has a wide range of uses in different fields, including chemistry, materials science, and industrial manufacturing, due to its unique properties and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 92074-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,7 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92074-11:
(7*9)+(6*2)+(5*0)+(4*7)+(3*4)+(2*1)+(1*1)=118
118 % 10 = 8
So 92074-11-8 is a valid CAS Registry Number.
92074-11-8Relevant articles and documents
N-ETHYLENEDIAMINES
Hu, Chunye,He, Ji-Gang,O'Brien, D. H.,Irgolic, K. J.
, p. 31 - 38 (2007/10/02)
A series of N-organosilylalkyl-substituted ethylenediamines, R3Si(CH2)nNHCH2CH2NH2 (R = CH3, C6H5 or 4-CH3C6H4; n = 1 or 3), were prepared by the reaction of haloalkylsilanes with ethylenediamine.The cleavage of a methyl group from silicon by concentrated sulfuric acid was used for the preparation of 1,3-bis-1,1,3,3-tetramethyldisiloxane.The proton and carbon-13 NMR spectra of these compounds are reported.
