63579-89-5 Usage
General Description
Triethyl pentane-1,3,5-tricarboxylate is a chemical compound with the molecular formula C17H28O6. It is an ester with three carboxyl groups attached to a pentane carbon chain, making it a triester. triethyl pentane-1,3,5-tricarboxylate is commonly used as a flavoring agent in the food industry, providing a fruity, rum-like aroma. It is also used in the production of fragrances and perfumes. Triethyl pentane-1,3,5-tricarboxylate is a colorless, clear liquid with a slightly sweet odor, and it is known for its low volatility and high stability, making it suitable for various applications in the fragrance and flavor industry.
Check Digit Verification of cas no
The CAS Registry Mumber 63579-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63579-89:
(7*6)+(6*3)+(5*5)+(4*7)+(3*9)+(2*8)+(1*9)=165
165 % 10 = 5
So 63579-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H24O6/c1-4-18-12(15)9-7-11(14(17)20-6-3)8-10-13(16)19-5-2/h11H,4-10H2,1-3H3
63579-89-5Relevant articles and documents
Yamada et al.
, p. 199,208, 211 (1968)
Stereoselective Synthesis of Cyclohexanes via an Iridium Catalyzed (5 + 1) Annulation Strategy
Akhtar, Wasim M.,Armstrong, Roly J.,Frost, James R.,Stevenson, Neil G.,Donohoe, Timothy J.
supporting information, p. 11916 - 11920 (2018/09/27)
An iridium catalyzed method for the synthesis of functionalized cyclohexanes from methyl ketones and 1,5-diols is described. This process operates by two sequential hydrogen borrowing reactions, providing direct access to multisubstituted cyclic products with high levels of stereocontrol. This methodology represents a novel (5 + 1) strategy for the stereoselective construction of the cyclohexane core.
FURTHER EXTENSIONS OF THE KINETIC ENOLATE METHOD FOR TERPENOID SYNTHESES
Ferrino, S. A.,Maldonado, L. A.
, p. 925 - 932 (2007/10/02)
New stereorandom syntheses of juvabione and dehydrojuvabione using kinetic enolates as synthons are described.
