1599-49-1 Usage
Description
4-METHYL-2-PENTYL-1,3-DIOXOLANE is an organic compound with a mild, fruity, pear-like odor. It is characterized by its taste threshold values and taste characteristics at 20 ppm, which are described as fruity, sweet, green, and waxy.
Uses
Used in Flavor and Fragrance Industry:
4-METHYL-2-PENTYL-1,3-DIOXOLANE is used as a flavoring agent for its fruity, sweet, and green waxy taste characteristics. Its mild, fruity, pear-like odor also makes it suitable for use as a fragrance ingredient in the perfumery industry.
Used in Chemical Synthesis:
4-METHYL-2-PENTYL-1,3-DIOXOLANE can be utilized as a building block or intermediate in the synthesis of various chemicals and pharmaceuticals, taking advantage of its unique chemical structure and properties.
Used in Research and Development:
Due to its distinctive chemical properties, 4-METHYL-2-PENTYL-1,3-DIOXOLANE may be employed in research and development for the creation of new compounds, materials, or processes in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1599-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1599-49:
(6*1)+(5*5)+(4*9)+(3*9)+(2*4)+(1*9)=111
111 % 10 = 1
So 1599-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O2/c1-3-4-5-6-9-10-7-8(2)11-9/h8-9H,3-7H2,1-2H3
1599-49-1Relevant articles and documents
Acetals and Ethers. 11. Solubility of Alkyl-Substituted 1,3-Dioxolanes and 1,3-Dioxanes in Water
Sokolowski, Adam,Burczyk, Bogdan,Oles, Jan
, p. 807 - 809 (1984)
2-Alkyl-1,3-dioxolanes, 2-alkyl-4-methyl-1,3-dioxolanes, and 2-alkyl-1,3-dioxanes (alkyl: n-C3H7, ...,n-C6H13) were synthesized and their solubilities in E10-4 M aqueous sodium bicarbonate solution at 293.2 K determined.The standard free energies for transfer from aqueous solution to pure liquid phase, ΔGto, were calculated from the solubility data and the contributions of given fragments of molecules to the free energy estimated.The fve-membered 1,3-dioxolane and six-membered 1,3-dioxane rings given fragments of molecules to the free energy contribution ΔGto, related to the cyclic fragments of the molecules, are +2.84 +/- 0.20 and +2.26 +/- 0.36 kJ mol-1, respectively.Their hydrophilicity is, however, much weaker than hat of the hydroxy group in normal alcohols.The 1,3-dioxolane ring bearing a methyl group at the C-4 atom has a markedly weaker hydrophilic character.
Synthesis of Aldehydes by Ozonolysis of Secondary Allyl
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Page/Page column 4, (2009/01/24)
The invention relates to a process for the preparation of an aldehyde from a secondary alcohol having a double bond in the alpha position, comprising the steps. a) provision of the alcohol,b) treatment of the alcohol with ozone.