153204-92-3 Usage
Uses
Used in Pharmaceutical Industry:
Silanamine, N-[(4-bromophenyl)methyl]-1,1,1-trimethyl-N-(trimethylsilyl)is used as a trimethylsilylating agent for protecting oxygen and nitrogen functional groups in organic synthesis, which is crucial in the development of new pharmaceutical compounds.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, Silanamine, N-[(4-bromophenyl)methyl]-1,1,1-trimethyl-N-(trimethylsilyl)serves as a trimethylsilylating agent, aiding in the synthesis of various agrochemicals by protecting functional groups during chemical reactions.
Used in Material Science:
Silanamine, N-[(4-bromophenyl)methyl]-1,1,1-trimethyl-N-(trimethylsilyl)is also utilized as a building block in the preparation of novel materials, contributing to the advancement of material science through its unique organosilicon structure.
Used in Synthesis of Biologically Active Molecules:
Furthermore, Silanamine, N-[(4-bromophenyl)methyl]-1,1,1-trimethyl-N-(trimethylsilyl)acts as a precursor in the formation of various biologically active molecules, playing a significant role in the creation of new compounds with potential therapeutic or other biological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 153204-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,0 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 153204-92:
(8*1)+(7*5)+(6*3)+(5*2)+(4*0)+(3*4)+(2*9)+(1*2)=103
103 % 10 = 3
So 153204-92-3 is a valid CAS Registry Number.
153204-92-3Relevant academic research and scientific papers
Cholic Acid as an Architectural Component in Biomimetic/Molecular Recognition Chemistry; Synthesis of the First "Cholaphanes".
Bonar-Law, Richard P.,Davis, Anthony P.
, p. 9829 - 9844 (2007/10/02)
The readily available steroid cholic acid (1) has several advantages as a precursor for extended, preorganised molecular frameworks.In the present work, full details are given for the conversion of 1 into ''cholaphanes'' 2a,b, the first macrocyclic steroi
