7534-55-6 Usage
Derivative of butanamine
Yes
It is a modified version of butanamine, with an additional phenylsilyl group attached.
Phenylsilyl group attachment
Fourth carbon of the butanamine chain
The phenylsilyl group is specifically attached to the fourth carbon atom in the butanamine chain.
Common use
Intermediate in organic synthesis
It is widely used as a building block or intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals.
Potential applications
Organic electronic devices
It has been studied for its potential use in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) and photovoltaic cells.
Importance
Diverse applications in organic chemistry
Due to its versatile structure and potential applications, 1-Butanamine, 4-(diethoxyphenylsilyl)is considered an important compound in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 7534-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,3 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7534-55:
(6*7)+(5*5)+(4*3)+(3*4)+(2*5)+(1*5)=106
106 % 10 = 6
So 7534-55-6 is a valid CAS Registry Number.
7534-55-6Relevant academic research and scientific papers
Process for making a silylisocyanurate
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, (2008/06/13)
This invention provides a process for making a silylorganocarbamate or a silylisocyanurate which process comprises reacting an aminosilane with a dialkyl carbonate, diaryl carbonate or a mixture thereof in the presence of a basic catalyst to obtain the silylorganocarbamate; optionally, neutralizing the basic catalyst and residual aminosilane with a neutralizing agent; and adding a cracking catalyst and heating at subatmospheric pressure to obtain the silylisocyanurate; or heating a silylorganocarbamate at a temperature sufficient for dissociation of the carbamate at subatmospheric pressure in the presence of a cracking catalyst and a timerization catalyst to obtain a silylisocyanurate.
