24402-72-0

Usage

Uses

Used in Dye and Optical Brightener Production:
N-ACETYL-4-NITRO-1-NAPHTHYLAMINE is used as a key intermediate in the synthesis of dyes and optical brighteners, contributing to the vibrant colors and enhanced visibility of various products.
Safety Precautions:
Due to its toxic and harmful nature, it is crucial to handle N-ACETYL-4-NITRO-1-NAPHTHYLAMINE with care. It should be stored in a cool, dry place and kept away from incompatible materials. Additionally, ingestion, inhalation, and skin or eye contact with N-ACETYL-4-NITRO-1-NAPHTHYLAMINE must be avoided to minimize health risks.

InChI:InChI=1/C12H10N2O3/c1-8(15)13-11-6-7-12(14(16)17)10-5-3-2-4-9(10)11/h2-7H,1H3,(H,13,15)

Upstream product

• 776-34-1 1-amino-4-nitronaphthalene 
• 108-24-7 acetic anhydride 
• 6921-26-2 1,4-dinitronaphthalene 
• 86-57-7 1-Nitronaphthalene 
• 134-32-7 1-amino-naphthalene 
• 575-36-0 1-acetamidonaphthalene 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 57-13-6 urea 

Downstream Products

• 7499-73-2 N-(4-bromo-2-nitronaphthalen-1-yl)acetamide 
• 91391-90-1 1-Amino-4-acetylaminonaphthalin 
• 776-34-1 1-amino-4-nitronaphthalene 
• 46874-39-9 1,4-N,N'-Diacetylnaphthylamin 

Relevant academic research and scientific papers

Direct cyanation of picolinamides using K4[Fe(CN)6] as the cyanide source

The efficient, simple, and environment-friendly route of direct cyanation of picolinamides has been developed with nontoxic K4[Fe(CN)6] as the cyanide source through Pdcatalyzed C-H bond activation. A series of N-(naphthalene-1- yl)picolinamide derivatives were successfully transformed to the corresponding cyanation products. The cyanation mechanism has also been speculated.

Regioselective ortho-nitration of N-phenyl carboxamides and primary anilines using bismuth nitrate/acetic anhydride

An efficient and one-pot synthetic method for the regioselective ortho-nitration of the N-phenyl carboxamides and primary anilines has been developed by using bismuth nitrate and acetic anhydride as the nitrating reagents. Reaction proceeds at room temperature and results in corresponding ortho-nitrated products in moderate to excellent yields. This method provides an operationally simple, regioselective, and efficient access to synthesize o-nitro anilines under the mild conditions.