68950-67-4

Basic information

• Product Name: 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE
• Synonyms: 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE;6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBALDEHYDE
• CAS NO: 68950-67-4
• Molecular Formula: C₁₂H₁₂O₃
• Molecular Weight: 204.22
• Mol File: 68950-67-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE(68950-67-4)
• EPA Substance Registry System: 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE(68950-67-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• HazardClass: IRRITANT
• Hazardous Substances Data: 68950-67-4(Hazardous Substances Data)

Usage

General Description

6-Methoxy-1-oxo-1,2,3,4-tetrahydro-[2]-naphthaldehyde is a chemical compound with the molecular formula C12H12O2. It is a colorless liquid with a molecular weight of 188.22 g/mol. 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE is used in the synthesis of a variety of pharmaceuticals and organic products. It is known for its aromatic and aldehyde properties, making it valuable in the production of fragrances and flavorings. Additionally, it is used in research and development of new chemical compounds due to its unique chemical properties. 6-METHOXY-1-OXO-1,2,3,4-TETRAHYDRO-[2]-NAPHTHALDEHYDE is also known for its potential application in the field of organic chemistry and chemical research.

Upstream product

• 109-94-4 formic acid ethyl ester 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 107-31-3 Methyl formate 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 501936-07-8 7-methoxy-4,5-dihydro-2H-benzo[g]indazole 
• 31184-53-9 4,5-dihydro-2H-benzo[g]indazol-7-ol 

Relevant articles and documents

The Quinary Catalyst-Substrate Complex Induced Construction of Spiro-Bridged or Cagelike Polyheterocyclic Compounds via a Substrate-Controlled Cascade Process

The asymmetric organocatalytic cascade reaction of cyclic β-oxo aldehydes to 2-hydroxycinnamaldehydes is developed. The bifunctional tertiary amine-thiourea catalyst was used in a rationally designed multiple catalysis where the asymmetric iminium catalysis and thiourea anion-binding catalysis were combined by carboxylate anion as a ternary catalytic system to form a quinary catalyst-substrate complex, providing an efficient protocol for the construction of enantioenriched spiro-bridged or cagelike polyheterocyclic compounds. The reuse of catalysts was also successfully realized.

Synthesis and structure-activity relationships of 2-amino-1- aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents

A series of aroylnaphthalene derivatives were prepared as bioisosteres of combrestatin A-4 and evaluated for anticancer activity. 2-Amino-1- aroylnaphthalene and 2-hydroxy-1-aroylnaphthalene, 9 and 8, respectively, showed strong antiproliferative activity

PYRIMIDINE DERIVATIVES AS 5HT2C RECEPTOR ANTAGONISTS

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