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1,2-Dioxolane-3-propanoicacid,3,5,5-trimethyl-,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

786658-57-9

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786658-57-9 Usage

Chemical structure

The compound consists of a dioxolane ring and a propanoic acid group with three methyl substituents.

Functional groups

Dioxolane ring, propanoic acid group, and methyl ester.

Molecular weight

Approximately 202.25 g/mol (calculated from the molecular formula).

Physical state

Likely a liquid at room temperature (based on the presence of a dioxolane ring and ester group).

Solvent properties

Commonly used as a solvent in organic synthesis.

Reactivity

Used as a reagent in organic synthesis, indicating its reactivity in various chemical reactions.

Pharmaceutical industry

Due to its unique chemical structure and properties.

Agricultural applications

Potential uses, but further research is needed.

Fragrance and flavor manufacturing

Possible uses in the production of fragrances and flavors.

Safety considerations

Further research and testing are necessary to fully understand the potential applications and safety considerations of this chemical.

Chemical classification

9CI (indicates a specific classification system used in chemistry, likely related to its structure and properties).

Check Digit Verification of cas no

The CAS Registry Mumber 786658-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,6,6,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 786658-57:
(8*7)+(7*8)+(6*6)+(5*6)+(4*5)+(3*8)+(2*5)+(1*7)=239
239 % 10 = 9
So 786658-57-9 is a valid CAS Registry Number.

786658-57-9Downstream Products

786658-57-9Relevant academic research and scientific papers

Curtius rearrangement and Wolff homologation of functionalized peroxides

Dussault, Patrick H.,Xu, Chunping

, p. 7455 - 7457 (2004)

The Curtius and Wolff rearrangements of peroxide-containing alkanoyl azides and diazoketones provide an efficient entry to peroxy-substituted amines, isocyanates, carbamates, and peroxyalkanoates.

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