1008531-78-9

Basic information

• Product Name: N-[(4-bromo-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide
• Synonyms: N-[(4-bromo-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide
• CAS NO: 1008531-78-9
• Molecular Weight: 370.246
• Mol File: 1008531-78-9.mol
• Article Data: 55

Chemical Properties

• CAS DataBase Reference: N-[(4-bromo-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(4-bromo-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide(1008531-78-9)
• EPA Substance Registry System: N-[(4-bromo-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide(1008531-78-9)

Safety Data

• Hazardous Substances Data: 1008531-78-9(Hazardous Substances Data)

Upstream product

• 60-35-5 acetamide 
• 1122-91-4 4-bromo-benzaldehyde 
• 135-19-3 β-naphthol 
• 873-75-6 4-bromobenzenemethanol 
• 75-05-8 acetonitrile 

Downstream Products

• 1190408-62-8 [1-(4-bromophenyl)-1,2-dihydro-3H-naphtho[1,2-e][1,3]oxazine-3-ylidene]malonaldehyde 

Relevant articles and documents

One-pot synthesis of 1-amidoalkyl-2-naphthols under solvent-free conditions

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Silica supported perchloric acid (HClO4-SiO2): an efficient and recyclable heterogeneous catalyst for the one-pot synthesis of amidoalkyl naphthols

An efficient and direct protocol for the preparation of amidoalkyl naphthols employing a multi-component and one-pot condensation reaction of 2-naphthol, aromatic aldehydes, and acetonitrile or acetamide in the presence of silica supported perchloric acid

Bronsted acidic ionic liquids as efficient catalysts for the synthesis of amidoalkyl naphthols

A simple, clean, and environmentally benign three-component process for the synthesis of amidoalkyl naphthols using Brnsted acidic ionic liquids as efficient catalysts in solution and under solvent-free conditions is described. Copyright Taylor & Francis

Nanomagnetite-supported molybdenum oxide (nanocat-Fe-Mo): an efficient green catalyst for multicomponent synthesis of amidoalkyl naphthols

Abstract: Magnetite (Fe3O4)-supported molybdenum oxide (MoO3) was synthesized from simple starting precursors in aqueous medium. The synthesized nanocat-Fe-Mo was analyzed using several techniques such as X-ray diffraction

β-Cyclodextrin-butane sulfonic acid: An efficient and reusable catalyst for the multicomponent synthesis of 1-amidoalkyl-2-naphthols under solvent-free conditions

β-cyclodextrin-butane sulfonic acid is reported to be an efficient catalyst for the one-pot synthesis of 1-amidoalkyl-2-naphthols by the multicomponent condensation of aromatic aldehydes, β-naphthol and amides under solvent-free conditions. The present methodology offers several advantages such as shorter reaction time, mild reaction conditions, a simple operational procedure and use of a recyclable catalyst.

ZS-1 Zeolite as a Highly Efficient and Reusable Catalyst for Facile Synthesis of 1-amidoalkyl-2-naphthols Under Solvent-Free Conditions

Efficient and reusable ZS-1 zeolite as a novel catalyst was successfully synthesized by the hydrothermal method. Characterizations of catalysts were carried out using diverse analysis techniques such as XRD, FT-IR, FESEM, EDAX, HRTEM, BET, and NH3/s

Preparation of 1-amidoalkyl-2-naphthol derivatives using barium phosphate nano-powders

Barium phosphate (Ba3(PO4)2) nano-powder was successfully synthesized via a simple precipitation route without any surfactant. The prepared nano-powder was applied for the facile synthesis of 1-amidoalkyl-2-naphthol derivatives using multi-component reaction of aldehydes, 2-naphthol and an amide (or urea) in high yields.

MCM-41-SO3H: A novel reusable nanocatalyst for synthesis of amidoalkyl naphthols under solvent-free conditions

Nanosized MCM-41-SO3H based on an ordered mesoporous material with covalently anchored sulfuric acid groups inside the mesochannels was used as an acid catalyst for synthesis of amidoalkyl naphthols in the multicomponent reaction of 2-naphthol,

Synthesis and characterization of a novel paramagnetic functionalized ionic liquid as a highly efficient catalyst in one-pot synthesis of 1-amidoalkyl-2-naphtols

A novel paramagnetic ionic liquid, 3-(2-hydroxyethyl)-1-methyl imidazolium bromotrichloro ferrate (III), was synthesized and exhibited high catalytic performance in the synthesis of 1-amidoalkyl-2-naphthols via one-pot three-component condensation reactio

Magnetic phosphonium ionic liquid: Application as a novel dual role acidic catalyst for synthesis of 2′-aminobenzothiazolomethylnaphthols and amidoalkyl naphthols

Abstract: In this investigation, a novel magnetic phosphonium ionic liquid (MPIL) was designed and synthesized through a two-step process. The resulting magnetic ionic liquid was fully characterized using different techniques including Fourier-transform i

Kal(SO4)2 12H2O as a recyclable lewis acid catalyst for synthesis of some amidoalkyl naphthols under solvent-free conditions

A general and practical one-pot synthesis of amidoalkyl naphthols derivatives using KAl(SO4)2 12H2O as catalyst is described. This method provides several advantages such as short reaction times, good yields, and simple wo

SbCl3-SiO 2 catalyzed simple and efficient one-pot synthesis of 1-amidoalkyl-2-naphthols under solvent-free conditions

Silica-supported antimony trichloride (SbCl3-SiO2) was found to be an inexpensive and effective catalyst for the one-pot three-component synthesis of 1-amidoalkyl-2-naphthols in high yields. The main advantages of the present approac

One-pot Synthesis of 1-Amidoalkyl-2-naphthols Catalyzed by Polyphosphoric Acid Supported on Silica-coated NiFe2O4 Nanoparticles

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A modified reaction for the preparation of amidoalkyl naphthols

An efficient synthesis of amidoalkyl naphthols using FeCl3·SiO2 as a heterogeneous catalyst is described. This thermal solvent-free procedure offers advantages such as shorter reaction times, simple work-up, excellent yields, and rec

Solvent free synthesis of amidoalkyl derivatives under green and convenient conditions

Amidoalkyl derivatives are significant compounds due to their application in the preparation of potent drugs and important biological compounds. In this context, we presented a new method for the synthesis of amido alkyl β-naphthol and amidoalky naphthoqu