2-Phthalimidoacetaldehyde Diethyl Acetal TCI P1229

Chemical Identity

CAS No.: 78902-09-7
PubChem: CID 315286·SID 87575325
Formula: C14H17NO4
Molecular weight: 263.29 g/mol
Purity: >95.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(2,2-diethoxyethyl)isoindole-1,3-dione
SMILES: CCOC(CN1C(=O)C2=CC=CC=C2C1=O)OCC
InChIKey: GEFXJJJQUSEHLV-UHFFFAOYSA-N

Rp 2.571.450,00

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2-Phthalimidoacetaldehyde Diethyl Acetal is a chemical compound widely used in organic reactions for the synthesis of complex molecules. Its unique structure, combining a phthalimido group with an acetal group, makes it a versatile building block in chemical synthesis. This compound is commonly utilized in laboratories for its ability to participate in various reactions such as hydrolysis, reduction, and nucleophilic reactions. Its role is critical in the development of heterocyclic compounds and bioactive molecules, making it an essential tool for researchers in multiple scientific disciplines.

The compound is favored for its stable chemical structure and controlled reactivity, allowing for precise manipulation in synthetic processes. Its resistance to degradation under normal conditions ensures long-term storage and repeated use without compromising its chemical integrity. This stability, combined with its reactivity, makes it a preferred choice for applications that require consistent performance and reliability. The compound's ability to undergo a variety of chemical transformations further enhances its utility in both academic and industrial research settings.

In Indonesian laboratories, 2-Phthalimidoacetaldehyde Diethyl Acetal is a popular reagent used in chemical, pharmaceutical, and biochemical research. It is frequently employed in experiments that require complex organic synthesis, particularly in the development of new drugs and bioactive compounds. Its availability in the local market supports ongoing research efforts, enabling scientists to conduct experiments efficiently and effectively.

Related TCI products

Organic synthesis of heterocyclic compounds due to its unique phthalimido and acetal functional groups.
Bioactive molecule development as it can participate in nucleophilic and reduction reactions.
Pharmaceutical research for the creation of new drug candidates through controlled chemical transformations.
Biochemical experiments where precise reactivity and stability are required for complex reaction sequences.
Academic research in chemistry and biochemistry for teaching and experimental purposes.

Brand	TCI
CAS number	78902-09-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain chemical stability. Due to its reactivity, it should be handled with care in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to incompatible substances, and ensure that storage conditions are consistent with standard laboratory safety protocols. Proper labeling and secure storage are essential to prevent accidental contamination or misuse.

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