1817-89-6 Usage
General Description
2-Ethoxypentane is a chemical compound consisting of a pentane molecule with an ethoxy (C2H5O-) group attached to one of its carbon atoms. It is also known as ethyl pentyl ether and has the chemical formula C7H16O. This chemical is a colorless liquid with a boiling point of 116-118°C and is commonly used as a solvent in various industrial applications. It is flammable and can be harmful if inhaled, ingested, or if it comes into contact with the skin and eyes. Additionally, 2-ethoxypentane is not readily biodegradable and has the potential to bioaccumulate in aquatic organisms. Therefore, proper handling and disposal procedures are necessary when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 1817-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1817-89:
(6*1)+(5*8)+(4*1)+(3*7)+(2*8)+(1*9)=96
96 % 10 = 6
So 1817-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-4-6-7(3)8-5-2/h7H,4-6H2,1-3H3
1817-89-6Relevant articles and documents
The continuous acid-catalysed etherification of aliphatic alcohols using stoichiometric quantities of dialkyl carbonates
Parrott, Andrew J.,Bourne, Richard A.,Gooden, Peter N.,Poliakoff, Martyn,Irvine, Derek J.,Bevinakatti, Han. S.
experimental part, p. 1420 - 1426 (2011/09/20)
A range of methyl and ethyl ethers of aliphatic alcohols have been synthesized cleanly in high yield by reacting the corresponding alcohol with dimethyl carbonate or diethyl carbonate over the solid acid catalyst, I-alumina. The reaction could be conducted at ambient pressure without the need for the large excess of dialkyl carbonate as previously reported in the literature. If the reaction was conducted at high pressure, the conversion of the starting alcohol was greatly reduced. However, high pressure CO2 can be used as the solvent without significant reduction in yield. This has implications for tandem reactions.
Hydrophobic vitamin B12. IV. Addition reactions of alcohols to olefins as catalyzed by hydrophobic vitamin B12 derivatives
Murakami,Hisaeda
, p. 2652 - 2658 (2007/10/02)
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