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Atomfair 1,3-Diacetoxybenzene Resorcinol diacetate C10H10O4

Description 1,3-Diacetoxybenzene (CAS No. 19806-17-8), also known as Resorcinol diacetate, is a high-purity organic compound with the molecular formula C10H10O4. This derivative of resorcinol features two acetyl groups, enhancing its stability and reactivity for specialized chemical applications. With an IUPAC name of (3-acetyloxyphenyl) acetate, it is widely utilized in pharmaceutical intermediates, polymer synthesis, and organic research. Our product is rigorously tested for purity and consistency, ensuring optimal performance in demanding laboratory and industrial processes. Available in various quantities, it is packaged under controlled conditions to maintain integrity and shelf life.

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Description

Description

1,3-Diacetoxybenzene (CAS No. 19806-17-8), also known as Resorcinol diacetate, is a high-purity organic compound with the molecular formula C10H10O4. This derivative of resorcinol features two acetyl groups, enhancing its stability and reactivity for specialized chemical applications. With an IUPAC name of (3-acetyloxyphenyl) acetate, it is widely utilized in pharmaceutical intermediates, polymer synthesis, and organic research. Our product is rigorously tested for purity and consistency, ensuring optimal performance in demanding laboratory and industrial processes. Available in various quantities, it is packaged under controlled conditions to maintain integrity and shelf life.

  • CAS No: 19806-17-8
  • Molecular Formula: C10H10O4
  • Molecular Weight: 194.18
  • Exact Mass: 194.05790880
  • Monoisotopic Mass: 194.05790880
  • IUPAC Name: (3-acetyloxyphenyl) acetate
  • SMILES: CC(=O)OC1=CC(=CC=C1)OC(=O)C
  • Synonyms: 1,3-Diacetoxybenzene, 108-58-7, Resorcinol diacetate, m-Phenylenediacetate, 1,3-Benzenediol, diacetate

Application

1,3-Diacetoxybenzene serves as a versatile intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is employed in polymer chemistry as a cross-linking agent or monomer due to its bifunctional reactivity. Researchers also utilize it in the development of UV stabilizers and specialty coatings. Its stability under mild conditions makes it suitable for controlled-release formulations and fine chemical manufacturing.

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