154845-34-8

Basic information

• Product Name: 3-Aminonaphthalene-2-carboxaldehyde
• Synonyms: 3-Aminonaphthalene-2-carboxaldehyde
• CAS NO: 154845-34-8
• Molecular Formula: C₁₁H₉NO
• Molecular Weight: 171.19526
• Mol File: 154845-34-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 370.8±25.0 °C(Predicted)
• Appearance: /
• Density: 1.245±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 2.85±0.10(Predicted)
• CAS DataBase Reference: 3-Aminonaphthalene-2-carboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Aminonaphthalene-2-carboxaldehyde(154845-34-8)
• EPA Substance Registry System: 3-Aminonaphthalene-2-carboxaldehyde(154845-34-8)

Safety Data

• Hazardous Substances Data: 154845-34-8(Hazardous Substances Data)

Upstream product

• 154845-27-9 3-(Trimethylacetamido)-2-naphthaldehyde 
• 21597-54-6 Methyl 3-amino-2-naphthoate 
• 141281-58-5 3-Amino-2-(hydroxymethyl)naphthalene 
• 154845-26-8 3-(Trimethylacetamido)-2-(hydroxymethyl)naphthalene 
• 5959-52-4 2-Amino-3-naphthoic acid 
• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 73428-05-4 3-nitro-2-naphthaldehyde 

Downstream Products

• 1426677-45-3 2-[(E)-2-phenylethenyl]benzo[g]quinoline 
• 260-36-6 1-azaanthracene 
• 844694-73-1 2-phenylbenzo[g]quinoline N-oxide 
• 110571-73-8 2-phenylbenzo[g]quinoline 

Relevant articles and documents

Cationic Iridium-Catalyzed Asymmetric Decarbonylative Aryl Addition of Aromatic Aldehydes to Bicyclic Alkenes

We report an unprecedented catalytic protocol for the enantioselective decarbonylative transformation of aryl aldehydes. In this process, the decarbonylation of aldehydes catalyzed by chiral iridium complexes enabled the formation of asymmetric C?C bonds

Asymmetric synthesis of isoquinolinonaphthyridines catalyzed by a chiral Br?nsted acid

A catalytic asymmetric method for the synthesis of chiral isoquinolinonaphthyridines has been developed. A chiral disulfonimide catalyzes a redox cyclization reaction between 2-methyl-3-aldehydeazaarenes and 1,2,3,4-tetrahydroisoquinolines to deliver a range of isoquinolinonaphthyridines with good to high yields (up to 91%) and up to 92:8 er.

Synthesis and spectral properties of Azahetero-aromatic derivatives of 2-styrylanthracene

Novel azaheteroaromatic derivatives of 2-styrylanthracene: 2-styrylbenzo[g]quinoline and 3-styryl- acridine were obtained from 3-nitro-2-naphthaldehyde and 2-bromo-4-methylbenzoic acid. Spectral properties of the new compounds were studied.