1817-89-6 Usage
Uses
Used in Chemical Industry:
2-Ethoxypentane is used as a solvent in various chemical processes for its ability to dissolve a wide range of substances. Its solubility properties make it a valuable component in the production of various chemicals and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Ethoxypentane serves as a solvent in the synthesis of drugs and active pharmaceutical ingredients. Its versatility in dissolving different compounds aids in the efficient production of medications.
Used in Cleaning Agents:
2-Ethoxypentane is utilized as a component in cleaning agents and degreasers due to its capacity to dissolve oils, greases, and other contaminants. This makes it suitable for industrial cleaning applications where the removal of stubborn residues is required.
Used in Paints and Coatings:
2-ETHOXYPENTANE is also employed in the formulation of paints and coatings, where it acts as a solvent to help in the application and drying process of these products. Its ability to dissolve various components contributes to the even distribution of pigments and binders in the paint.
Used in Fragrance Industry:
In the fragrance industry, 2-Ethoxypentane is used as a solvent for essential oils and other aromatic compounds. Its solubility properties allow for the creation of concentrated and stable fragrances.
Used in Adhesives and Sealants:
2-ETHOXYPENTANE is also used in the production of adhesives and sealants, where it helps in the dissolution of various components to create a consistent and effective bonding material.
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 academic research and scientific papers
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.
Nucleophilic Displacement with Heterocycles as Leaving Groups. Part 16. Reactions of Secondary Alkyl Primary Amines with 5,6,8,9-Tetrahydro-7-phenyldibenzoxanthylium Trifluoromethanesulphonate to give Intermediates Solvolysing without Rearrangement
Katritzky, Alan R.,Lopez-Rodriguez, Maria L.,Keay, James G.,King, Roy W.
, p. 165 - 170 (2007/10/02)
Representative secondary alkyl primary amines R1R2CHNH2 react with the title pyrylium cation in acetic acid, alcohols, phenols, and NN-dimethylaniline acting as nucleophilic solvents to give O- and C-(secondary alkyl) products.Absence of carbenium ion rearrangements is consistent with reaction via intimate ion-molecule pairs formed rapidly from the corresponding pyridinium cations.
