CAS 17720-64-8

2-(Acetyloxy)-1H-isoindole-1,3(2H)-dione

Description:

2-(Acetyloxy)-1H-isoindole-1,3(2H)-dione, also known by its CAS number 17720-64-8, is a chemical compound characterized by its isoindole structure, which features a fused benzene and pyrrole ring system. This compound contains an acetyloxy group, contributing to its reactivity and potential applications in organic synthesis. It typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics. The presence of the dione functional groups indicates that it can participate in various chemical reactions, such as nucleophilic additions and condensation reactions. Its unique structure allows it to exhibit biological activity, making it of interest in medicinal chemistry. Additionally, the compound may be sensitive to light and moisture, necessitating careful handling and storage conditions. Overall, 2-(Acetyloxy)-1H-isoindole-1,3(2H)-dione is a versatile compound with potential applications in pharmaceuticals and organic synthesis.

Formula: C₁₀H₇NO₄

InChI: InChI=1S/C10H7NO4/c1-6(12)15-11-9(13)7-4-2-3-5-8(7)10(11)14/h2-5H,1H3

InChI key: InChIKey=IJRNYIWWGDQEIY-UHFFFAOYSA-N

SMILES: O=C1C=2C(C(=O)N1OC(C)=O)=CC=CC2

Synonyms:

• 2-(Acetyloxy)-1H-isoindole-1,3(2H)-dione
• NSC 101749
• N-Acetoxyphthalimide
• Phthalimide, N-acetoxy-
• 1H-Isoindole-1,3(2H)-dione, 2-(acetyloxy)-

1H-Isoindole-1,3(2H)-dione, 2-(acetyloxy)-

CAS: 17720-64-8

Formula: C₁₀H₇NO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 205.1669

Ref: IN-DA00256S

1,3-Dioxoisoindolin-2-yl acetate

CAS: 17720-64-8

1,3-Dioxoisoindolin-2-yl acetate

Purity: 98%

Molecular weight: 205.17g/mol

Ref: 54-OR96141

1,3-Dioxoisoindolin-2-yl acetate

CAS: 17720-64-8

Purity: 98%

Color and Shape: Solid

Molecular weight: 205.1690063

Ref: 10-F783913

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl acetate

CAS: 17720-64-8

1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl acetate is a reactive intermediate that can be used as a starting material for the synthesis of other organic compounds. It is synthesized by the reaction of an acid with an aldehyde or ketone in the presence of a base. The rate of this reaction depends on the functional groups present in both reactants and their relative concentrations. This intermediate can be converted to another chemical compound through various reactions, including hydroxymethylation, decarboxylation and oxidation. This chemical has been used as a cocatalyst for the production of 5-hydroxymethylfurfural (HMF).

Formula: C₁₀H₇NO₄

Purity: Min. 95%

Molecular weight: 205.17 g/mol

Ref: 3D-SAA72064