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CAS 17295-11-3

Methyl 6-Hydroxy-2-naphthoate TCI H1053

Methyl 6-Hydroxy-2-naphthoate TCI H1053

Chemical Identity

CAS No.
17295-11-3
Formula
C12H10O3
Molecular weight
202.21 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 6-hydroxynaphthalene-2-carboxylate
SMILES
COC(=O)C1=CC2=C(C=C1)C=C(C=C2)O
InChIKey
UKZOPQRTQJERQC-UHFFFAOYSA-N
PubChem
CID 390995
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Methyl 6-Hydroxy-2-naphthoate is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it serves as a versatile intermediate in various synthetic pathways. Its role is particularly significant in reactions that require the introduction of hydroxyl groups into molecular structures. This compound is commonly utilized in chemical laboratories for its ability to participate in multiple reaction types, including esterification and substitution reactions. Its chemical stability and reactivity under controlled conditions make it a valuable reagent for researchers and students alike.

The compound’s chemical properties, such as its ability to act as a hydroxyl donor, make it a preferred choice in synthetic chemistry. Its molecular structure allows it to interact with a variety of functional groups, enabling the formation of more complex organic molecules. The compound’s stability under standard laboratory conditions ensures that it remains a reliable reagent for repeated use. Its compatibility with different reagents and solvents further enhances its utility in diverse chemical applications. These characteristics position it as an essential component in both academic and industrial research environments.

In Indonesian laboratories, Methyl 6-Hydroxy-2-naphthoate is frequently used in chemical research, pharmaceutical development, and organic synthesis. Its availability and cost-effectiveness make it a popular choice for researchers and students conducting experiments. The compound’s versatility in various reaction types supports its application in a wide range of laboratory processes, contributing to the advancement of chemical studies in Indonesia.

  • Synthesis of heterocyclic compounds for pharmaceutical development due to its ability to introduce hydroxyl groups into molecular structures.
  • Esterification reactions where it acts as a hydroxyl donor, enabling the formation of ester functional groups.
  • Organic synthesis applications where its reactivity and compatibility with various reagents support the creation of complex molecules.
  • Research in chemical engineering for the development of new materials and chemical processes.
  • Educational experiments in chemistry courses to demonstrate the principles of organic synthesis and functional group chemistry.

Brand TCI
CAS number 17295-11-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid, crystalline appearance
Storage Store in a cool, dry place away from direct sunlight and moisture

Methyl 6-Hydroxy-2-naphthoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. The storage area should be free from direct sunlight and sources of heat to avoid degradation. When handling the compound, it is advisable to use appropriate personal protective equipment such as gloves and safety goggles. Due to its reactivity, it should be stored separately from strong oxidizing agents and incompatible substances. Proper labeling of containers ensures safe handling and minimizes the risk of accidental exposure in laboratory settings.

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