219685-15-1

Basic information

• Product Name: 4-Formylnaphthalene-1-carboxylic acid
• Synonyms: 4-Formylnaphthalene-1-carboxylic acid;4-forMyl-1-naphthoic acid
• CAS NO: 219685-15-1
• Molecular Formula: C₁₂H₈O₃
• Molecular Weight: 200.19012
• Mol File: 219685-15-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Formylnaphthalene-1-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Formylnaphthalene-1-carboxylic acid(219685-15-1)
• EPA Substance Registry System: 4-Formylnaphthalene-1-carboxylic acid(219685-15-1)

Safety Data

• Hazardous Substances Data: 219685-15-1(Hazardous Substances Data)

Upstream product

• 62855-40-7 methyl 4-formyl-1-naphthalenecarboxylate 
• 4488-40-8 4-Methyl-1-naphthoic acid 
• 30236-02-3 4-(bromomethyl)-naphthalene-1-carboxylic acid 
• 57322-46-0 4-(hydroxymethyl)-naphthalene-1-carboxylic acid 
• 105904-00-5 methyl 4-hydroxymethyl-1-naphthoate 
• 35615-98-6 methyl 4-methyl-1-naphthalenecarboxylate 
• 50672-84-9 4-bromo-1-naphthaldehyde 

Downstream Products

• 219685-16-2 4-[(3-Chloro-4-hydroxybenzoyl)hydrazonomethyl]naphthoic Acid 

Relevant articles and documents

Method for preparing oxazoline insecticide arforaging intermediate

The invention discloses a method for preparing an oxazoline insecticide arfamarin intermediate. The intermediate is 4-formyl-naphthalene-1-carboxylic acid, and compared with a synthesis route of US6613942B1, the synthesis route of the oxazoline insecticide arfamarin is simple. According to the method provided by some embodiments of the invention, through exploration, the reaction steps are shortened from three steps to one step, so the oxazoline insecticide arforlaana intermediate product with qualified purity can be obtained. The intermediate control steps are simplified, meanwhile, the product yield is increased, and industrial production is easier.

Glucagon antagonists/inverse agonists

Non-peptide compounds comprising a central hydrazide motif and methods for the synthesis thereof are disclosed. The compounds act to antagonize the action of the glucagon peptide hormone.