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N-[(4-methyl-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 332174-63-7 Structure
  • Basic information

    1. Product Name: N-[(4-methyl-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide
    2. Synonyms: N-[(4-methyl-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide
    3. CAS NO:332174-63-7
    4. Molecular Formula:
    5. Molecular Weight: 305.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 332174-63-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-[(4-methyl-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(4-methyl-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide(332174-63-7)
    11. EPA Substance Registry System: N-[(4-methyl-phenyl)-(2-hydroxy-naphthalen-1-yl)-methyl]acetamide(332174-63-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 332174-63-7(Hazardous Substances Data)

332174-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332174-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,1,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 332174-63:
(8*3)+(7*3)+(6*2)+(5*1)+(4*7)+(3*4)+(2*6)+(1*3)=117
117 % 10 = 7
So 332174-63-7 is a valid CAS Registry Number.

332174-63-7Relevant articles and documents

Triethylamine-bonded sulfonic acid ([Et3N-SO3H]Cl): A highly efficient and homogeneous catalyst for the condensation of 2-naphthol with arylaldehydes and amides (alkyl carbamates or thioamides)

Zare, Abdolkarim,Akbarzadeh, Shayesteh,Foroozani, Elmira,Kaveh, Hamideh,Moosavi-Zare, Ahmad Reza,Hasaninejad, Alireza,Mokhlesi, Mohammad,Beyzavi, Mohammad Hassan,Zolfigol, Mohammad Ali

, p. 259 - 272 (2012)

Ionic liquid triethylamine-bonded sulfonic acid ([Et3N-SO 3H]Cl, N,N-diethyl-N-sulfoethanammonium chloride) is utilized as a highly efficient, inexpensive and homogeneous catalyst to promote the following one-pot multi-component organic transformations under solvent-free conditions: (i) the condensation of 2-naphthol with arylaldehydes and amides leading to 1-amidoalkyl-2-naphthols, (ii) the reaction of 2- naphthol with aromatic aldehydes and alkyl carbamates to produce 1-carbamatoalkyl-2-naphthols, and (iii) the condensation between 2-naphthol, arylaldehydes and thioamides leading to 1-thioamidoalkyl-2- naphthols. High yields, short reaction times, efficiency, generality, clean process, simple methodology, low cost, easy work-up, ease of preparation of the catalyst, and environmentally benign conditions are some advantages of the protocols.

Bovine bone-derived natural hydroxyapatite-supported ZnCl2 as a sustainable high efficiency heterogeneous biocatalyst for synthesizing amidoalkyl naphthols

Azzallou, Rachid,Geesi, Mohammed H.,Kaiba, Abdellah,Kamal, Mehnaz,Lazar, Sa?d,Mamouni, Rachid,Ouerghi, Oussama,Riadi, Yassine,Taleb, Mohamed Ait,Villain, Sylvie

, (2022/01/06)

Waste-derived materials have emerged as promising catalysts to meet the requirements for green chemistry. Catalysts and solvents are recognized as the most important components of the 12 principles of green chemistry. The reactivity of members of this cla

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

Dipake, Sudarshan S.,Gadekar, Sachin P.,Gaikwad, Suresh T.,Lande, Machhindra K.,Rajbhoj, Anjali S.,Thombre, Premkumar B.

, (2021/06/14)

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 and characterization of nano-Co-[4-chlorophenyl-salicylaldimine-methyl pyranopyrazole]Cl2 as a new Schiff base complex and catalyst for the solvent-free synthesis of 1-amidoalkyl-2-naphthols

Moosavi-Zare, Ahmad Reza,Goudarziafshar, Hamid,Nooraei, Fatemeh

, (2019/11/13)

By the reaction of 4-chlorobenzaldehyde with ethyl acetoacetate, malononitrile, and hydrazine hydrate, 6-amino-4-(4-chlorophenyl)-3-methyl-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile was prepared and then reacted with salicylaldehyde and CoCl2/s

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

Torabi, Morteza,Yarie, Meysam,Zolfigol, Mohammad Ali,Azizian, Saeid

, p. 891 - 907 (2019/11/03)

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

Chitosan-SO3H (CTSA) an efficient and biodegradable polymeric catalyst for the synthesis of 4,4′-(arylmethylene)bis(1H-pyrazol-5-ol) and α-amidoalkyl-β-naphthol’s

Patil, Paresh G.,Sehlangia, Suman,More, Dhananjay H.

supporting information, p. 1696 - 1711 (2020/05/25)

An efficient, green procedure for the synthesis of 4,4′-(arylmethylene)bis(1H-pyrazol-5-ol) and α-amidoalkyl-β-naphthol’s using biodegradable polymeric catalyst chitosan-SO3H (CTSA), is operationally easy to prepare by mixing chitosan and chlor

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

Bankar, Swapnil R.,Shelke, Sharad N.

, p. 3507 - 3521 (2018/02/21)

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

Caffeine-H3PO4: a novel acidic catalyst for various one-pot multicomponent reactions

Saghanezhad, Seyyed Jafar,Sayahi, Mohammad Hosein,Imanifar, Iman,Mombeni, Mostafa,Deris Hamood, Sajedeh

, p. 6521 - 6536 (2017/10/06)

Caffeine-H3PO4 along with caffeine-HClO4 and caffeine-HNO3 have been prepared and applied for one-pot preparation of bis(indolyl) methanes, 4,4′-(arylmethylene) bis(1H-pyrazol-5-ols), 3,3′-(arylmethylene) bis(4-hydroxycoumarins), 2,4,5-trisubstituted imidazoles, 1‐amidoalkyl‐2‐naphthols, and polyhydroquinolines. The catalysts were characterized using Fourier-transform infrared (FTIR) spectroscopy, 1H and 13C nuclear magnetic resonance (NMR), powder X-ray diffraction (PXRD) analysis, thermogravimetric analysis (TGA), and liquid chromatography (LC)–mass spectroscopy (MS) techniques. The results indicated high product yield, short reaction time, facile separation of catalyst, and easy work-up procedure, suggesting that caffeine-H3PO4 can be considered to be an efficient acidic catalyst for organic transformations.

Homopiperazine sulfamic acid functionalized mesoporous silica nanoparticles (MSNs-HPZ-SO3H) as an efficient catalyst for one-pot synthesis of 1-amidoalkyl-2-naphthols

Nasresfahani, Zahra,Kassaee, Mohammad Zaman,Eidi, Esmaiel

, p. 4720 - 4726 (2016/06/09)

Mesoporous silica nanoparticles are efficiently functionalized with homopiperazine sulfamic acid. The resulting MSNs-HPZ-SO3H is employed as a nanocatalyst in one-pot synthesis of 1-amidoalkyl-2-naphthols, through three-component condensation r

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

Taghrir, Hadi,Ghashang, Majid,Biregan, Mohammad Najafi

, p. 119 - 126 (2016/01/26)

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.

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