113522-44-4 Usage
Common uses
Crosslinking agent for epoxy resins
Curing agent for polyurethane coatings
Chemical structure
Contains two amine groups (-NH2)
Has phenylmethyl (-C6H5CH2) groups attached to the nitrogen atoms
Features trimethylsilyl (-Si(CH3)3) groups attached to the nitrogen atoms
Functionality
Utilized in various chemical reactions due to the presence of amine groups
Increases flexibility and toughness of polymers
Protection
Trimethylsilyl groups provide protection for the reactive amine groups
Allows for controlled and selective reactions
Applications
Production of adhesives
Coatings
Other polymeric materials
Check Digit Verification of cas no
The CAS Registry Mumber 113522-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,2 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113522-44:
(8*1)+(7*1)+(6*3)+(5*5)+(4*2)+(3*2)+(2*4)+(1*4)=84
84 % 10 = 4
So 113522-44-4 is a valid CAS Registry Number.
113522-44-4Relevant academic research and scientific papers
MACROCYCLISATION EN SERIES LACTONE, THIOLACTONE et LACTAME a MOTIF ETHYLENE DIOXY. EFFETS de MATRICE du SILICIUM et de l'ETAIN
Leygue, N.,Picard, C.,Tisnes, P.,Cazaux, L.
, p. 5845 - 5856 (2007/10/02)
The orientation of the macrocyclization reaction leading to the di or tetrafunctional titled compounds has been studied for 12 and 24 membered rings containing ethylene dioxy moieties.The reactions were carried out from not activated diol, dithiol or diamine and from their silyl and stannyl derivatives.They were not performed at high dilution.The intracyclic oxygen atoms had a strong influence on the orientation of the cyclisation towards the monomer.However, it was also possible to obtain the dimeric forms with yields ranging from 10 to 40percent.
