61920-32-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-(cyclohex-3-en-1-yl)-4-methyl-1,3-dioxolane is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure contributes to the development of new and effective compounds for medical and agricultural applications.
Used in Chemical Reactions as a Solvent:
2-(cyclohex-3-en-1-yl)-4-methyl-1,3-dioxolane serves as a solvent in a range of chemical reactions, facilitating the process and improving the efficiency of the reactions. Its properties make it a valuable component in the synthesis of other organic compounds.
Used in Perfumes as a Fragrance Ingredient:
2-(cyclohex-3-en-1-yl)-4-methyl-1,3-dioxolane is employed in the fragrance industry, where it is used to create and enhance the scents of perfumes. Its aromatic properties contribute to the complexity and appeal of fragrances.
Used in Food Products as a Flavoring Agent:
In the food industry, 2-(cyclohex-3-en-1-yl)-4-methyl-1,3-dioxolane is used as a flavoring agent to impart or enhance the taste of various food products. Its ability to add unique flavors makes it a sought-after ingredient in the culinary world.
Used in the Production of Other Organic Compounds:
2-(cyclohex-3-en-1-yl)-4-methyl-1,3-dioxolane also functions as an intermediate in the manufacturing process of other organic compounds, showcasing its versatility and importance in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 61920-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,2 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61920-32:
(7*6)+(6*1)+(5*9)+(4*2)+(3*0)+(2*3)+(1*2)=109
109 % 10 = 9
So 61920-32-9 is a valid CAS Registry Number.
61920-32-9Relevant academic research and scientific papers
Chemistry of Dioxacyclanes: X. Synthesis and Properties of Chlorinated 1,3-Dioxolanes Derived from 4-Cyclohexenecarbaldehydes
Kerimov
, p. 131 - 134 (2007/10/03)
4-Cyclohexenecarbaldehyde and its 2-methyl-, 4-methyl-, and 2,4-dimethyl derivatives were reacted with 1,2-diols [1,2-propanediol and 3-chloro-, 3-(2-chloroethoxy)-, and 3-(2-chloro-1-chloromethylethoxy-1,2-propandiol] to synthesize the corresponding 2,4-
Chemistry of dioxacycloalkanes: VII. Synthesis and properties of substituted 1,3-dioxolanes derived from carbocyclic aldehydes
Kerimov
, p. 136 - 140 (2007/10/03)
Reactions of 3-cyclohexenecarbaldehyde, 6-methyl-3-cyclohexenecarbaldehyde, bicyclo[2.2.1]-hept-5-ene-endo-2-carbaldehyde, and benzaldehyde with 1,2-propanediol and 3-chloro-1,2-propanediol gave the corresponding 2,4-substituted 1,3-dioxolanes. Their reactions with peroxyacetic acid, bromine, dichlorocarbene, and nucleophiles were studied. The effect of the substituents in the diol and aldehyde on their relative reactivity is discussed.
CHEMISTRY OF DIOXACYCLANES. V. SYNTHESIS OF 1,3-DIOXOLANE DERIVATIVES FROM 3-CYCLOHEXENE-1-CARBALDEHYDE AND BICYCLOHEPT-5-ENE-2-CARBALDEHYDE AND STUDY OF THEIR PROPERTIES
Kerimov, A. Kh.,Babaev, M. G.,Alieva, E. S.,Mishiev, D. E.
, p. 2160 - 2164 (2007/10/02)
The reaction of 3-cyclohexene-1-carbaldehyde and bicyclohept-5-ene-2-carbaldehyde with 1,2-propanediol and its 3-chloro, 3-(2-chloroethoxy), and 3-(2-chloro-1-chloromethylethoxy) derivatives gave the corresponding 2,4-substituted 1,3-dioxolanes.The
