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Atomfair 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2,6-dichlorobenzoate C15H7Cl2NO4
Description 1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl 2,6-dichlorobenzoate (CAS No. 2248284-29-7) is a high-purity synthetic organic compound with the molecular formula C15H7Cl2NO4. This specialized chemical features a unique isoindole-1,3-dione scaffold esterified with a 2,6-dichlorobenzoate group, making it a valuable intermediate for pharmaceutical and agrochemical research. With a molecular weight of 336.13 g/mol, this compound is supplied as a crystalline solid with ??95% purity (HPLC). Its structural complexity and reactive sites enable diverse derivatization opportunities for drug discovery and material science applications. Store in a cool, dry place under inert conditions to ensure stability.
Description
Description
1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl 2,6-dichlorobenzoate (CAS No. 2248284-29-7) is a high-purity synthetic organic compound with the molecular formula C15H7Cl2NO4. This specialized chemical features a unique isoindole-1,3-dione scaffold esterified with a 2,6-dichlorobenzoate group, making it a valuable intermediate for pharmaceutical and agrochemical research. With a molecular weight of 336.13 g/mol, this compound is supplied as a crystalline solid with ??95% purity (HPLC). Its structural complexity and reactive sites enable diverse derivatization opportunities for drug discovery and material science applications. Store in a cool, dry place under inert conditions to ensure stability.
- CAS No: 2248284-29-7
- Molecular Formula: C15H7Cl2NO4
- Molecular Weight: 336.1
- Exact Mass: 334.9752131
- Monoisotopic Mass: 334.9752131
- IUPAC Name: (1,3-dioxoisoindol-2-yl) 2,6-dichlorobenzoate
- SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)OC(=O)C3=C(C=CC=C3Cl)Cl
- Synonyms: SCHEMBL13479736, 2248284-29-7, EN300-6514277, 1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl 2,6-dichlorobenzoate
Application
This compound serves as a versatile building block in medicinal chemistry, particularly for the synthesis of isoindole-1,3-dione derivatives with potential biological activity. Researchers utilize it in developing small-molecule inhibitors and protease-targeting agents. The dichlorobenzoate moiety enhances lipophilicity, making it valuable for pharmacokinetic optimization studies. It’s also investigated as a precursor for fluorescent dyes and polymer modifiers due to its conjugated system.
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