5621-09-0 Usage
General Description
DIMETHYLDI-N-PROPOXYSILANE is a chemical compound that belongs to the organosilicon family and is commonly used as a coupling agent in the production of silane-based materials. It consists of two methyl groups, a propoxy group, and a silane group, making it a versatile component for various industrial applications. It is used as a silane coupling agent in the production of adhesives, coatings, and sealants, as well as in the modification of inorganic surfaces to improve adhesion and compatibility with organic materials. DIMETHYLDI-N-PROPOXYSILANE is known for its ability to enhance the mechanical and chemical properties of materials and is widely used in the manufacturing of plastics, rubber, and composites. This chemical is also utilized in the production of silicone-based products, providing them with improved water and moisture resistance.
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.