N-Acetylphthalimide TCI A0108

Chemical Identity

CAS No.: 1971-49-9
PubChem: CID 243267·SID 87561803
Formula: C10H7NO3
Molecular weight: 189.17 g/mol
Purity: >98.0%(N)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-acetylisoindole-1,3-dione
SMILES: CC(=O)N1C(=O)C2=CC=CC=C2C1=O
InChIKey: INZUQGFQRYAKQQ-UHFFFAOYSA-N

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TCI A0108 N-Acetylphthalimide (CAS 1971-49-9) is an organic compound belonging to the N-acyl imide class: a phthalimide derivative whose nitrogen atom carries an acetyl group. In the laboratory it is classed as a non-heterocyclic building block, meaning it serves as a starting material or intermediate reagent in the construction of more complex molecules. Its most common association is with acetyl-group transfer and the synthesis of nitrogen-containing derivatives, which is why synthetic organic chemists often consider it.

The structural feature that makes this compound attractive is the bond between the imide nitrogen and the acyl group. A bond of this kind is generally more reactive than that of an ordinary amide, so compounds of this type are often used as a relatively controlled source of acetyl groups. The rigid, aromatic phthalimide framework also contributes structural stability and makes reactions easy to follow by thin-layer chromatography or spectroscopy. This makes the material well suited to stepwise synthetic routes that call for a well-defined reagent.

For laboratories in Indonesia, from university organic chemistry laboratories and research centers to development laboratories in industry, this reagent fits routine synthetic and research work. It is supplied under the TCI brand through AMI Scientific, so users can select it for method development, teaching syntheses and exploratory projects that need a defined acetyl-transfer reagent. Its place within the non-heterocyclic building block range makes it a practical addition to a laboratory's reagent inventory.

Related TCI products

Acetyl group transfer: the N-acyl imide bond is generally more reactive than a standard amide, so this compound can serve as a relatively controlled source of acetyl groups in synthetic reactions.
Synthesis of nitrogen derivatives: as a phthalimide derivative, it suits researchers building nitrogen-containing target molecules, where the imide framework gives a defined and well-characterized starting point.
Building block for multistep synthesis: as a non-heterocyclic building block, it works as a starting material or intermediate reagent when more complex molecules are assembled step by step in the laboratory.
Reaction monitoring studies: the rigid aromatic phthalimide skeleton makes progress easy to follow by thin-layer chromatography and spectroscopy, which helps when optimizing and checking each synthetic step.
Teaching and training in organic synthesis: the compound illustrates imide reactivity and acyl transfer clearly, so university laboratories can use it to demonstrate these concepts in practical synthetic exercises.

Brand	TCI
CAS number	1971-49-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	please refer to the product listing or consult AMI Scientific for available sizes
Physical form	please refer to the supplier's label and safety data sheet
Storage	—

Product code: A0108

Store the product in its original, tightly closed container in a cool, dry, well-ventilated place, away from moisture, heat and incompatible materials. Because N-acyl imides can be sensitive to water, keep the container sealed whenever it is not in use. Follow the storage instructions on the supplier's label and safety data sheet. Use standard laboratory precautions: wear gloves, safety glasses and a lab coat, and handle the material in a fume hood or well-ventilated area to avoid inhaling dust. Avoid contact with skin and eyes, and wash hands after handling. Dispose of waste according to institutional and local regulations.

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