1333248-11-5 Usage
Description
(3,4-dimethoxyphenoxy)trimethylsilane is an organosilicon compound that is a clear, colorless liquid with a molecular formula of C11H18O3Si. It is known for its versatility and is commonly used in various industries due to the presence of trimethylsilane.
Uses
Used in Organic Synthesis:
(3,4-dimethoxyphenoxy)trimethylsilane is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions and improve the efficiency of the synthesis process.
Used in Self-Assembled Monolayers:
(3,4-dimethoxyphenoxy)trimethylsilane is used as a protective agent in the fabrication of self-assembled monolayers, providing a stable and uniform coating on surfaces.
Used in Manufacturing of Polymers:
(3,4-dimethoxyphenoxy)trimethylsilane is used in the manufacturing of polymers for its ability to enhance the properties of the final product, such as stability, durability, and performance.
Used in Coatings Industry:
(3,4-dimethoxyphenoxy)trimethylsilane is used in the coatings industry to improve the adhesion, durability, and overall performance of coatings on various surfaces.
Used in Biomedical Materials:
(3,4-dimethoxyphenoxy)trimethylsilane is used in the development of biomedical materials for its biocompatibility and ability to improve the properties of these materials, such as their stability and performance in medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1333248-11-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,4 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333248-11:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*4)+(3*8)+(2*1)+(1*1)=125
125 % 10 = 5
So 1333248-11-5 is a valid CAS Registry Number.
1333248-11-5Relevant articles and documents
Convergent Total Synthesis of (±)-Apomorphine via Benzyne Chemistry: Insights into the Mechanisms Involved in the Key Step
Muraca, Ana Carolina A.,Perecim, Givago P.,Rodrigues, Alessandro,Raminelli, Cristiano
, p. 3546 - 3557 (2017/08/15)
Convergent total synthesis of (±)-apomorphine hydrochloride was accomplished by an approach that employs in the key step a sequence of transformations involving a [4+2]-cycloaddition reaction followed by a hydrogen migration. Through this sequence of transformations, the desired aporphine core was obtained regioselectively in 75% isolated yield. Since only one regioisomer was produced in the key step of the synthesis, a polar [4+2]-cycloaddition mechanism was proposed. Furthermore, NMR experiments and theoretical calculations were carried out to elucidate the hydrogen migration mechanism. (±)-Apomorphine hydrochloride was achieved after 9 steps in an overall yield of 8% involving benzyne chemistry.
