18135-04-1 Usage
Uses
Used in Organic Synthesis:
2-(TriMethylsilyl)ethylaMine is employed as a reagent or catalyst in the process of organic synthesis. Its amine and trimethylsilyl groups contribute to its effectiveness in facilitating chemical reactions, making it a popular choice among chemists for a range of applications.
Used in Chemical Research:
In the realm of chemical research, 2-(TriMethylsilyl)ethylaMine is utilized for its unique properties, which can be harnessed to explore new reaction pathways and develop novel compounds. Its versatility in chemical procedures makes it a valuable tool for advancing scientific understanding and innovation.
Used in Pharmaceutical Industry:
2-(TriMethylsilyl)ethylaMine is used as a building block or intermediate in the synthesis of various pharmaceutical compounds. Its ability to participate in a wide array of chemical reactions allows for the creation of new drug candidates with potential therapeutic applications.
Used in Material Science:
In material science, 2-(TriMethylsilyl)ethylaMine is used as a component in the development of new materials with specific properties. Its involvement in chemical reactions can lead to the creation of materials with tailored characteristics, such as improved stability or enhanced reactivity, for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 18135-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18135-04:
(7*1)+(6*8)+(5*1)+(4*3)+(3*5)+(2*0)+(1*4)=91
91 % 10 = 1
So 18135-04-1 is a valid CAS Registry Number.
18135-04-1Relevant articles and documents
N,N-Bis(trimethylsilyl)methoxymethylamine as a Convenient Synthetic Equivalent for +CH2NH2: Primary Aminomethylation of Organometallic Compounds
Morimoto, Toshiaki,Takahashi, Toshio,Sekiya, Minoru
, p. 794 - 795 (2007/10/02)
The introduction of the primary aminomethyl unit at carbon through N,N-bis(trimethylsilyl)aminomethylation of Grignard and organolithium compounds can be achieved in good yield using N,N-bis(trimethylsilyl)methoxymethylamine (1).
