Ethyl 3-Hydroxy-2-naphthoate TCI E1249

Chemical Identity

Other names: 3-Hydroxy-2-naphthoic Acid Ethyl Ester
CAS No.: 7163-25-9
PubChem: CID 737040·SID 354335274
Formula: C13H12O3
Molecular weight: 216.24 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 3-hydroxynaphthalene-2-carboxylate
SMILES: CCOC(=O)C1=CC2=CC=CC=C2C=C1O
InChIKey: CVEOWBRXZJEZRQ-UHFFFAOYSA-N
MDL: MDL00220608

Rp 928.200,00

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Ethyl 3-Hydroxy-2-naphthoate is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a building block in chemical reactions, it serves as a versatile reagent that can participate in various synthetic pathways. This compound is commonly found in chemical laboratories as a precursor for the preparation of organic compounds containing naphthalene structures. Its role in chemical synthesis is crucial due to its ability to act as a hydroxyl group donor, enabling reactions with a range of other reagents.

The compound’s molecular structure is stable and allows for easy manipulation in chemical reactions. Its hydroxyl group makes it suitable for reactions such as esterification, hydrolysis, and substitution. These chemical properties make it a preferred choice for researchers seeking a flexible and reactive starting material. The compound’s reactivity and structural simplicity contribute to its popularity in both academic and industrial research environments.

In Indonesian laboratories, Ethyl 3-Hydroxy-2-naphthoate is extensively used in organic chemistry research, particularly in the development of pharmaceutical compounds and industrial chemicals. It is also utilized in educational settings to train students in synthesis techniques and chemical handling. Its application spans across various research fields, making it an essential component in the chemical supply chain for Indonesian laboratories.

Related TCI products

Pharmaceutical synthesis for the development of new drug compounds due to its reactivity and structural versatility.
Organic chemistry research involving naphthalene-based molecules for the creation of complex chemical structures.
Esterification reactions in the production of ester derivatives for use in fragrance and flavor industries.
Educational purposes in teaching students about synthetic chemistry and functional group transformations.
Industrial chemical synthesis for the production of specialty chemicals and intermediates.

Brand	TCI
CAS number	7163-25-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid depending on the batch and supplier
Storage	Store in a cool, dry place away from direct sunlight and moisture

Ethyl 3-Hydroxy-2-naphthoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. The compound should be stored away from incompatible substances such as strong oxidizers or acids. Laboratory personnel should handle it with appropriate personal protective equipment, including gloves and safety goggles. Regular monitoring of storage conditions is essential to ensure the compound remains in optimal condition for use. Proper labeling and storage practices help minimize the risk of accidental exposure or contamination.

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