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Atomfair 1,3-Diethoxypropane C7H16O2
Description 1,3-Diethoxypropane (CAS No. 3459-83-4) is a high-purity organic compound with the molecular formula C7H16O2. This colorless liquid is widely used as a versatile reagent in organic synthesis, particularly as a protecting group for aldehydes and ketones. Its IUPAC name, 1,3-diethoxypropane , reflects its symmetrical ether structure, which enhances its stability and reactivity in various chemical transformations. With a molecular weight of 132.20 g/mol, this compound is characterized by its low volatility and excellent solubility in common organic solvents. Ideal for laboratory and industrial applications, our 1,3-Diethoxypropane is rigorously tested to ensure ??98% purity, meeting the stringent requirements of researchers…
Description
Description
1,3-Diethoxypropane (CAS No. 3459-83-4) is a high-purity organic compound with the molecular formula C7H16O2. This colorless liquid is widely used as a versatile reagent in organic synthesis, particularly as a protecting group for aldehydes and ketones. Its IUPAC name, 1,3-diethoxypropane, reflects its symmetrical ether structure, which enhances its stability and reactivity in various chemical transformations. With a molecular weight of 132.20 g/mol, this compound is characterized by its low volatility and excellent solubility in common organic solvents. Ideal for laboratory and industrial applications, our 1,3-Diethoxypropane is rigorously tested to ensure ??98% purity, meeting the stringent requirements of researchers and scientists. Proper storage under inert conditions is recommended to maintain its integrity.
- CAS No: 3459-83-4
- Molecular Formula: C7H16O2
- Molecular Weight: 132.20
- Exact Mass: 132.115029749
- Monoisotopic Mass: 132.115029749
- IUPAC Name: 1,3-diethoxypropane
- SMILES: CCOCCCOCC
- Synonyms: 1,3-Diethoxypropane, 3459-83-4, DTXSID00188150, EC 413-140-6, DTXCID30110641
Application
1,3-Diethoxypropane is primarily employed as a protecting group reagent for carbonyl compounds in organic synthesis, enabling selective transformations. It serves as a key intermediate in the preparation of fragrances, pharmaceuticals, and specialty chemicals. Additionally, this compound is utilized in the synthesis of heterocyclic compounds and as a solvent or co-solvent in various reactions. Its stability under acidic conditions makes it valuable for acetal formation and other protective strategies.
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