1971-81-9

Usage

Uses

Used in Chemical Synthesis:
4-Dimethylamino-1-naphthaldehyde is used as a key intermediate in the synthesis of various organic compounds, particularly those with pharmaceutical or chemical applications. Its unique structure allows for further functionalization and modification, making it a versatile building block in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Dimethylamino-1-naphthaldehyde is used as a starting material for the development of new drugs. Its chemical properties enable the creation of novel drug candidates with potential therapeutic benefits.
Used in Dye Manufacturing:
4-Dimethylamino-1-naphthaldehyde is also utilized in the production of dyes, specifically as a precursor for the synthesis of leuco base. This leuco base is then used to create various dyes with different color properties, contributing to the diversity of colorants available in the market.
Used in Analytical Chemistry:
Due to its unique chemical structure, 4-Dimethylamino-1-naphthaldehyde can be employed in analytical chemistry as a reagent or a derivatizing agent. It can be used to detect or quantify specific compounds through colorimetric or fluorometric methods, providing valuable information in research and quality control processes.

InChI:InChI=1/C13H13NO/c1-14(2)13-8-7-10(9-15)11-5-3-4-6-12(11)13/h3-9H,1-2H3

Upstream product

• 86-56-6 N,N-dimethyl-1-naphthalenamine 
• 2591-86-8 N-Formylpiperidine 
• 59557-93-6 4-bromo-1-(N,N-dimethylamino)naphthalene 
• 149-73-5 trimethyl orthoformate 
• 3377-92-2 vinyl pivalate 
• 1131-80-2 (E)-3-(N,N-dimethylamino)-1-phenyl-2-propen-1-one 
• 18103-98-5 (E)-3-(dimethylamino)-1-p-tolylprop-2-en-1-one 
• 3506-37-4 (E)-1-phenyl-3-(piperidin-1-yl)prop-2-en-1-one 
• 2298-07-9 4-Bromo-1-naphthylamine 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 142599-30-2 4-dimethylamino-1-trans-styryl-naphthalene 
• 1642812-32-5 N,N-dimethyl-4-(1,4,5-triphenyl-1H-imidazol-2-yl)naphthalen-1-amine 
• 1620959-65-0 N,N-dimethyl-4-(1-phenyl-1H-phenanthro[9,10-d]imidazol-2-yl)naphthalen-1-amine 
• 1026167-95-2 {4-[Bis-(4-pyrrolidin-1-yl-phenyl)-methyl]-naphthalen-1-yl}-dimethyl-amine 

Relevant academic research and scientific papers

Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization

An expedient [5 + 1] annulation method via Rh(III)-catalyzed C-H bond functionalization of enaminones to synthesize polyaromatic rings is described. The reaction tolerates a broad range of functional groups and offers a new entry to construct polycyclic a

Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization

An expedient [5 + 1] annulation method via Rh(III)-catalyzed C-H bond functionalization of enaminones to synthesize polyaromatic rings is described. The reaction tolerates a broad range of functional groups and offers a new entry to construct polycyclic a

A simple TiCl4 promoted arylation of orthoformate and benzyl ethers by N,N-dialkylarylamines

N,N-Dialkylarylamines react with trimethyl orthoformate and TiCl4 under ambient conditions to give the corresponding formyl derivatives in 75-89% yields, whereas the corresponding arylated products are obtained from benzyl ethers and acetals in 42-78% yields.

Resonance-stabilized α-naphthylmethyl carbocations and spiro compounds based thereon: VII. Transformations of α-naphthylmethyl carbocations stabilized by one electron-donor group or peri-fused heteroring

1-Hydroxymethyl- and 1-alkoxymethylnaphthalenes containing dimethylamino and methoxy groups or a heteroring in positions 4 and 5 react with protic and Lewis acids to give 1-naphthylmethyl carbocations. Reactions of the latter with the initial alcohol molecule lead to the formation of oligomerization or dehydrogenation (to aldehyde) products or the corresponding dinaphthylmethanes. In some cases, the process was accompanied by cyclodimerization to form cyclohexadienone spiro derivatives in a small yield. Pleiades Publishing, Inc., 2006.

The effects of cyclic terminal groups in di- and tri-arylmethane dyes. Part 2.1 Steric and electronic effects in derivatives of Victoria Blue

The effects of N-alkyl and heterocycloalkyl substitueras on the light absorption properties of a range of novel dyes based on the 1-naphthyl analogue of Crystal Violet, Victoria Blue, have been investigated. Interaction between the N-terminal group and th