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CAS 7442-52-6

:

methyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate

Description:
Methyl 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate, identified by the CAS number 7442-52-6, is an organic compound characterized by its complex bicyclic structure. It features a naphthalene core, which is a fused ring system, and includes a ketone functional group (the 1-oxo group) and an ester functional group (the methyl carboxylate). This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is known for its potential applications in organic synthesis and as an intermediate in the production of various chemical compounds. The presence of both the ketone and ester functionalities allows for diverse reactivity, making it useful in various chemical reactions, including nucleophilic additions and condensation reactions. Additionally, its structural characteristics may impart specific physical properties, such as solubility in organic solvents and varying degrees of volatility. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C12H12O3
InChI:InChI=1/C12H12O3/c1-15-12(14)10-7-6-8-4-2-3-5-9(8)11(10)13/h2-5,10H,6-7H2,1H3
SMILES:COC(=O)C1CCc2ccccc2C1=O
Synonyms:
  • METHYL 1-OXO-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBOXYLATE
  • 1,2,3,4-tetrahydro-2-carbomethoxy-1-oxonaphthalene
  • 2-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-1-oxo-, Methyl ester
  • methyl 1-oxo-3,4-dihydro-2H-naphthalene-2-carboxylate
  • 1,2,3,4-tetrahydro-1-oxo-2-Naphthalenecarboxylic acid methyl ester
  • METHYL 1-OXO-1
  • 1-OXO-1,2,3,4-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID METHYL ESTER
  • 4-TETRAHYDRONAPHTHALENE-2-CARBOXYLATE
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