1708-35-6 Usage
Uses
Used in the Paint and Coating Industry:
1,3-Dioxolane-4-methanol, 2-hexylis utilized as a solvent to enhance the performance and application of paints and coatings. Its properties contribute to improved flow, leveling, and drying characteristics, ensuring a high-quality finish.
Used in the Adhesive Industry:
In the adhesive sector, 1,3-Dioxolane-4-methanol, 2-hexylserves as a solvent that aids in the formulation of adhesives with specific bonding properties. It helps in achieving the desired viscosity and performance for various substrate applications.
Used as a Precursor in Chemical and Pharmaceutical Production:
1,3-Dioxolane-4-methanol, 2-hexylis employed as a precursor in the synthesis of other chemicals and pharmaceuticals. Its role in the production process is crucial for creating intermediates that are essential for developing final products with specific therapeutic or functional uses.
Safety Considerations:
While 1,3-Dioxolane-4-methanol, 2-hexylis favored for its low toxicity, it is imperative to handle 1,3-Dioxolane-4-methanol, 2-hexyl- with care and implement appropriate safety measures. This includes using personal protective equipment, ensuring proper ventilation during use, and adhering to guidelines to prevent exposure and any potential adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 1708-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1708-35:
(6*1)+(5*7)+(4*0)+(3*8)+(2*3)+(1*5)=76
76 % 10 = 6
So 1708-35-6 is a valid CAS Registry Number.
1708-35-6Relevant academic research and scientific papers
Method for the Synthesis of Cyclic Acetals by the Reactive Extraction of a Polyol in a Concentrated Solution
-
Page/Page column 5, (2010/05/13)
A method for the synthesis of cyclic acetals comprises reacting at least one carbonyl-function compound selected from aldehydes, ketones, and/or linear acetals, on a polyol in a concentrated aqueous solution exceeding 20 wt % in a reactor containing an acidic catalyst. The carbonyl-function compound is selected so that the cyclic acetal obtained has a water solubility lower than 20000 mg/kg. During the catalytic reaction for the cyclic acetal synthesis, at least one portion of the organic phase containing the cyclic acetal is separated. The acidic catalysis is either homogeneous when using a water-soluble strong acid, or heterogeneous when using a solid acid such as a resin, a zeolite, or any appropriately acidified solid. The extractive reaction method can be used for obtaining high conversions and selectivity.
