10586-16-0 Usage
Uses
Used in Organic Synthesis:
2,4-Bis[(trimethylsilyl)oxy]benzoic acid trimethylsilyl ester is used as a protecting group for carboxylic acids in organic synthesis. The presence of the trimethylsilyl ester groups allows for the protection of the carboxylic acid functionality, facilitating further synthetic transformations and reactions.
Used in Medicinal and Pharmaceutical Chemistry:
In the field of medicinal and pharmaceutical chemistry, 2,4-Bis[(trimethylsilyl)oxy]benzoic acid trimethylsilyl ester is used as a key intermediate in the synthesis of complex organic molecules. Its properties make it a valuable tool for the development of new drugs and pharmaceutical compounds.
Used in the Production of Complex Organic Molecules:
2,4-Bis[(trimethylsilyl)oxy]benzoic acid trimethylsilyl ester is used as a building block in the production of complex organic molecules. Its stability and protection of the carboxylic acid functionality make it an essential component in the synthesis of a wide range of chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 10586-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10586-16:
(7*1)+(6*0)+(5*5)+(4*8)+(3*6)+(2*1)+(1*6)=90
90 % 10 = 0
So 10586-16-0 is a valid CAS Registry Number.
10586-16-0Relevant academic research and scientific papers
Synthesis of trimethylsilyl carboxylates by HMDS under solvent-free conditions
Jereb, Marjan,Lakner, Janja
, p. 5713 - 5723 (2016/08/23)
A broad set of structurally different carboxylic acids were transformed into their trimethylsilyl esters with HMDS in a practically completely solvent-free process, while a catalytic amount of iodine was required in some cases. The process has several advantages over the known methods: untreated reactants, air atmosphere, mild and neutral conditions, no evolution of hydrogen halide, no need of an additional base, low amount of waste, completely without chromatography, low consumption of energy, and operational simplicity.
