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TCI

CAS 2150-46-1

Methyl 2,5-Dihydroxybenzoate TCI M2006

Methyl 2,5-Dihydroxybenzoate TCI M2006

Chemical Identity

CAS No.
2150-46-1
PubChem
CID 75077·SID 87560590
Formula
C8H8O4
Molecular weight
168.15 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 2,5-dihydroxybenzoate
SMILES
COC(=O)C1=C(C=CC(=C1)O)O
InChIKey
XGDPKUKRQHHZTH-UHFFFAOYSA-N
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Methyl 2,5-Dihydroxybenzoate is a chemical compound widely used in laboratory settings for its versatility in chemical reactions. As a building block in organic chemistry, it plays a crucial role in the synthesis of aromatic compounds and their derivatives. This compound is particularly valuable for researchers and students engaged in chemical experimentation, offering a reliable starting material for various synthetic pathways. Its presence in laboratory applications highlights its importance in both academic and industrial research environments.

The compound's chemical structure is stable and reactive, making it a preferred choice for a range of chemical processes. Its ability to undergo substitution and oxidation reactions makes it suitable for a variety of synthetic strategies. The non-heterocyclic nature of Methyl 2,5-Dihydroxybenzoate simplifies its use in reactions that do not involve heterocyclic structures. These properties make it a versatile reagent in both basic and advanced chemical experiments.

In Indonesian laboratories, Methyl 2,5-Dihydroxybenzoate is commonly used by researchers and students for scientific research, practical exams, and the development of new chemical materials. Its availability in the local market ensures accessibility for educational and research purposes. The compound's applications span across multiple fields, including pharmaceuticals, dyes, and analytical chemistry, supporting a wide range of experimental needs.

  • Synthesis of aromatic compounds for drug development and chemical material innovation due to its reactivity and structural versatility.
  • Oxidation and substitution reactions in organic synthesis because of its stability and compatibility with various reagents.
  • Colorant production in industrial applications where its chemical properties contribute to the formation of dye molecules.
  • Analytical chemistry experiments as a reference compound for testing and calibration processes.
  • Educational purposes in academic institutions for teaching and practical training in chemical synthesis techniques.

Brand TCI
CAS number 2150-46-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

Methyl 2,5-Dihydroxybenzoate 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 moisture absorption and contamination. Avoid exposure to direct sunlight and high humidity, as these conditions may affect its reactivity and purity. In laboratory settings, it is advisable to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Proper ventilation should be maintained when working with this material to minimize inhalation risks. Its non-heterocyclic nature ensures it is generally compatible with most laboratory equipment and reagents, making it a safe and reliable choice for a wide range of chemical applications.

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