71590-32-4

Basic information

• Product Name: N-(6-bromo-[2]naphthyl)-acetamide
• Synonyms: N-(6-bromo-[2]naphthyl)-acetamide
• CAS NO: 71590-32-4
• Molecular Weight: 264.121
• Mol File: 71590-32-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N-(6-bromo-[2]naphthyl)-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(6-bromo-[2]naphthyl)-acetamide(71590-32-4)
• EPA Substance Registry System: N-(6-bromo-[2]naphthyl)-acetamide(71590-32-4)

Safety Data

• Hazardous Substances Data: 71590-32-4(Hazardous Substances Data)

Usage

Description

N-(6-bromo-[2]naphthyl)-acetamide is a chemical compound that belongs to the class of acetamides. It is derived from the substitution of a bromine atom at the 6th position of a naphthyl group, which is then attached to an acetamide functional group. This unique structure and properties make it suitable for use as a building block in the synthesis of other complex organic molecules. Additionally, it may exhibit certain biological activities or interactions that could make it useful in medicinal chemistry or drug development. Overall, N-(6-bromo-[2]naphthyl)-acetamide is a versatile chemical that shows promise for a range of practical applications.

Uses

Used in Pharmaceutical Industry:
N-(6-bromo-[2]naphthyl)-acetamide is used as a building block for the synthesis of complex organic molecules, which can be further developed into potential pharmaceutical compounds. Its unique structure allows for the exploration of various applications in medicinal chemistry and drug development.
Used in Agrochemical Industry:
N-(6-bromo-[2]naphthyl)-acetamide is used as a starting material for the development of new agrochemicals. Its chemical properties can be exploited to create compounds with specific pesticidal, herbicidal, or fungicidal activities, contributing to the advancement of crop protection strategies.
Used in Materials Science:
N-(6-bromo-[2]naphthyl)-acetamide is used as a component in the development of novel materials with specific properties. Its unique structure can be utilized to create materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity, for various applications in materials science.

Upstream product

• 591253-73-5 6-bromo-1-aminonaphthalene 
• 108-24-7 acetic anhydride 
• 5773-80-8 6-bromo-2-naphthoic acid 
• 71590-31-3 6-bromo-2-aminonaphthalene hydrochloride 
• 13720-04-2 1,6-dibromonaphthalen-2-amine 
• 7499-66-3 6-Bromonaphthalen-2-amine 

Downstream Products

• 1241377-74-1 6-bromo-naphthalene-1,2-diamine 
• 1334312-52-5 MK-8325 
• 1334314-20-3 C₄₃H₅₄N₈O₆Si 
• 1334313-80-2 C₂₉H₃₂N₆Si 
• 1334313-79-9 C₃₉H₄₈N₆O₄Si 
• 1146206-16-7 C₂₃H₂₀N₂O₄ 
• 131707-40-9 6-bromo-1-nitronaphthalen-2-amine 
• 22082-94-6 2-bromo-6-phenylnaphthalene 
• 116668-47-4 6-amino-2-naphthoic acid 
• 855930-17-5 N-acetyl-1-nitro-6-bromonaphthalene 
• 7499-66-3 6-Bromonaphthalen-2-amine 

Relevant articles and documents

Industrial preparation method of 6-bromonaphthalene-1, 2-diamine

The invention discloses an industrial preparation method of 6-bromonaphthalene-1, 2-diamine. The method comprises the following steps of: S1, making a compound III react with acetic anhydride in the presence of alkali and a catalyst to obtain a compound IV; S2, in the presence of acetic anhydride and nitric acid, taking acetic acid as a reaction solvent, performing reacting and purifying on the compound IV obtained in the step S1 to generate a compound V; S3, adding the compound V obtained in the above step into a solvent for dissolving the compound V, then adding a metal reducing agent and an ammonium chloride solution, heating to carry out a reaction for 6h, performing centrifugal filtering after finishing the reaction to obtain a filtrate, washing the filtrate with a sodium chloride solution, and performing concentrating to obtain a compound VI; and S4, adding the compound VI obtained in the previous step into a methanol solution, dropwise adding strong acid, replacing the solvent after finishing the reaction, performing crystallizing and filtering to obtain a compound 8. According to the method, the process is optimized, large-scale production can be achieved, applied materials are all commercial reagents, the cost is reduced, and the operation convenience is improved.

COMPOUNDS AS HEPATITIS C VIRUS INHIBITORS AND PHARMACEUTICAL USES THEREOF

The invention provides compounds as hepatitis C virus inhibitors and pharmaceutical uses thereof. Specifically, the invention provides compounds of Formula (I) or a stereoisomer, a tautomer, an enantiomer, an N-oxide, a hydrate, a solvate, a metabolite, a

FUSED TRICYCLIC COMPOUNDS AND DERIVATIVES THEREOF USEFUL FOR THE TREATMENT OF VIRAL DISEASES

The present invention relates to novel fused tricyclic compounds, compositions comprising at least one fused tricyclic compound, and methods of using fused tricyclic compounds for treating or preventing a viral infection or a virus-related disorder in a patient.