5621-09-0 Usage
Uses
Used in Adhesives, Coatings, and Sealants Industry:
DIMETHYLDI-N-PROPOXYSILANE is used as a silane coupling agent to enhance the mechanical and chemical properties of adhesives, coatings, and sealants. It improves adhesion and compatibility between inorganic surfaces and organic materials, resulting in stronger and more durable products.
Used in Plastics, Rubber, and Composites Manufacturing:
DIMETHYLDI-N-PROPOXYSILANE is utilized as a coupling agent in the manufacturing of plastics, rubber, and composites. Its presence helps to improve the overall performance and durability of these materials, making them more resistant to mechanical stress and environmental factors.
Used in Silicone-based Products Production:
DIMETHYLDI-N-PROPOXYSILANE is used in the production of silicone-based products to provide them with improved water and moisture resistance. This enhancement makes these products more suitable for applications where resistance to water and moisture is crucial, such as in construction, automotive, and electronics industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5621-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5621-09:
(6*5)+(5*6)+(4*2)+(3*1)+(2*0)+(1*9)=80
80 % 10 = 0
So 5621-09-0 is a valid CAS Registry Number.
5621-09-0Relevant articles and documents
Iodine- or Iodine Monobromide-Catalyzed Alkoxy-Alkoxy Exchange Reactions of Alkylalkoxysilanes: Formation of the Catalyst-Alkoxysilane Complexes and the Reaction Mechanism
Ito, Katsuko,Ibaraki, Takeshi
, p. 2853 - 2858 (2007/10/02)
The formation of charge-transfer complexes of iodine and of iodine monobromide with alcohols and alkoxysilanes has been established spectroscopically, and the formation constants of iodine-ethoxytriethylsilane and iodine-diethoxydimethylsilane complexes has been determined as 0.55+/-0.01 and 0.61+/-0.02, respectively.On the basis of these observations and the kinetic information recently reported, the previously proposed mechanism for the iodine or iodine monobromide catalyzed alkoxy-alkoxy exchange reactions of alkoxysilanes is dicussed afresh.It has been confirmed that a mechanism involving a four-centered transition state containing a CT-complex is most favorable.