Atomfair 2-[(4-chlorobenzoyl)oxy]-1H-isoindole-1,3(2H)-dione C15H8ClNO4

Description 2-[(4-chlorobenzoyl)oxy]-1H-isoindole-1,3(2H)-dione (CAS No. 63591-89-9) is a high-purity organic compound with the molecular formula C15H8ClNO4. Also known as (1,3-dioxoisoindol-2-yl) 4-chlorobenzoate, this specialized chemical is designed for advanced research and industrial applications. Its unique structure combines a phthalimide core with a 4-chlorobenzoate ester, making it a valuable intermediate in synthetic chemistry. This product is rigorously tested for purity and consistency, ensuring reliable performance in your experiments. Ideal for pharmaceutical development, material science, and organic synthesis, it is available in various quantities to meet your research needs.

Description

2-[(4-chlorobenzoyl)oxy]-1H-isoindole-1,3(2H)-dione (CAS No. 63591-89-9) is a high-purity organic compound with the molecular formula C₁₅H₈ClNO₄. Also known as (1,3-dioxoisoindol-2-yl) 4-chlorobenzoate, this specialized chemical is designed for advanced research and industrial applications. Its unique structure combines a phthalimide core with a 4-chlorobenzoate ester, making it a valuable intermediate in synthetic chemistry. This product is rigorously tested for purity and consistency, ensuring reliable performance in your experiments. Ideal for pharmaceutical development, material science, and organic synthesis, it is available in various quantities to meet your research needs.

CAS No: 63591-89-9
Molecular Formula: C15H8ClNO4
Molecular Weight: 301.68
Exact Mass: 301.0141854
Monoisotopic Mass: 301.0141854
IUPAC Name: (1,3-dioxoisoindol-2-yl) 4-chlorobenzoate
SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)OC(=O)C3=CC=C(C=C3)Cl
Synonyms: 63591-89-9, 1,3-dioxoisoindolin-2-yl 4-chlorobenzoate, 1H-Isoindole-1,3(2H)-dione, 2-[(4-chlorobenzoyl)oxy]-, 2-[(4-chlorobenzoyl)oxy]-1H-isoindole-1,3(2H)-dione, SCHEMBL11073957

Application

This compound serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceutical agents and specialty chemicals. Its reactive ester group enables efficient coupling reactions, while the phthalimide moiety offers opportunities for further functionalization. Researchers utilize it in the study of heterocyclic compounds and as a building block for complex molecular architectures. Its stability and well-defined reactivity make it suitable for controlled reactions in both academic and industrial settings.

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