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Carbonic acid di-sec-butyl ester, also known as di-sec-butyl carbonate, is an organic compound with the chemical formula C9H18O3. It is a colorless, volatile liquid that is soluble in most organic solvents. This ester is formed by the reaction of carbonic acid with two molecules of sec-butanol, resulting in the formation of an ester linkage between the carbonic acid and the sec-butanol molecules. Carbonic acid di-sec-butyl ester is primarily used as a solvent, particularly in the production of polymers and as a component in various chemical processes. It is also used as a fuel additive and a component in some types of lubricants. Due to its low toxicity and high boiling point, it is considered a safer alternative to other solvents in certain applications.

623-63-2

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623-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 623-63-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 623-63:
(5*6)+(4*2)+(3*3)+(2*6)+(1*3)=62
62 % 10 = 2
So 623-63-2 is a valid CAS Registry Number.

623-63-2Downstream Products

623-63-2Relevant academic research and scientific papers

Direct condensation reaction of carbon dioxide with alcohols using trisubstituted phosphine-carbon tetrabromide-base system as a condensing agent

Kadokawa, Jun-Ichi,Habu, Hideyuki

, p. 2205 - 2208 (2007/10/03)

This paper describes the preparation of carbonates by the direct condensation of CO2 with alcohols using a trisubstituted phosphine-carbon tetrabromide-base system as a condensing agent. The yield of dibenzyl carbonate from CO2 and benzyl alcohol was at most 90.7%. The reaction of CO2 with the other primary alcohols such as methanol, ethanol, butan-1-ol, hexan-1-ol, allyl alcohol, and ethylene glycol also gave corresponding carbonates in relatively high yields, whereas yields of carbonates from CO2 and secondary alcohols were low. Copyright 1999 by the Royal Society of Chemistry.

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