N-Acetyl-1-aminonaphthalene

  • CAS：575-36-0
  • purity：99%
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Details

Factory supply good quality N-Acetyl-1-aminonaphthalene 575-36-0 with stock

  • Molecular Formula: C12H11NO
  • Molecular Weight: 185.225
  • Appearance/Colour: White crystalline powder. 
  • Vapor Pressure: 4.73E-07mmHg at 25°C 
  • Melting Point: 156-160 °C 
  • Refractive Index: 1.667 
  • Boiling Point: 413.6 °C at 760 mmHg 
  • PKA: 15.12±0.30(Predicted) 
  • Flash Point: 245.6 °C 
  • PSA： 29.10000 
  • Density: 1.182g/cm3 
  • LogP: 2.87120 

N-Acetyl-1-aminonaphthalene(Cas 575-36-0) Usage

InChI:InChI=1/C12H11NO/c1-9(14)13-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3,(H,13,14)

575-36-0 Relevant articles

Design, synthesis and biological evaluation of some novel diastereoselective β-lactams bearing 2-mercaptobenzothiazole and benzoquinoline

Borazjani, Nassim,Jarrahpour, Aliasghar,Rad, Javad Ameri,Mohkam, Milad,Behzadi, Maryam,Ghasemi, Younes,Mirzaeinia, Somayyeh,Karbalaei-Heidari, Hamid Reza,Ghanbari, Mohammad Mehdi,Batta, Gyula,Turos, Edward

, p. 329 - 339 (2019)

We report the synthesis of some novel β-...

Synthesis, spectral, and electrochemical properties of meso-5,10,15,20- tetrakis (2'-chlorobenzoquinolin-3'-yl)porphyrins

Prasath,Bhavana

, p. 525 - 530 (2012)

The synthesis, characterization, and red...

Intramolecular Participation by an Amide Group in Ester Hydrolysis

Hibbert, Frank,Sellens, Rowena J.

, p. 399 - 402 (1988)

The rate coefficient for hydrolysis of 1...

Preparation method of acetamide compound

-

Paragraph 0035-0047, (2021/05/19)

The invention discloses a preparation me...

Chlorination Reaction of Aromatic Compounds and Unsaturated Carbon-Carbon Bonds with Chlorine on Demand

Liu, Feng,Wu, Na,Cheng, Xu

supporting information, p. 3015 - 3020 (2021/05/05)

Chlorination with chlorine is straightfo...

Silver(I) Promoted the C4-H Bond Phosphonation of 1-Naphthylamine Derivatives with H-Phosphonates

Zhao, Lixiao,Sun, Mengmeng,Yang, Fan,Wu, Yangjie

, p. 11519 - 11530 (2021/09/02)

A simple and efficient protocol for silv...

Chemoselective reduction of nitroarenes, N-acetylation of arylamines, and one-pot reductive acetylation of nitroarenes using carbon-supported palladium catalytic system in water

Zeynizadeh, Behzad,Mohammad Aminzadeh, Farkhondeh,Mousavi, Hossein

, p. 3289 - 3312 (2021/05/11)

Developing and/or modifying fundamental ...

575-36-0 Process route

α-naphthol
90-15-3

α-naphthol

ammonium acetate
631-61-8,92206-38-7

ammonium acetate

1-acetamidonaphthalene
575-36-0

1-acetamidonaphthalene

N,N-di(naphth-1-yl)amine
737-89-3

N,N-di(naphth-1-yl)amine

1-amino-naphthalene
134-32-7

1-amino-naphthalene

Conditions
Conditions Yield
at 270 - 280 ℃;
1-tetralone oxime
3349-64-2,68253-36-1,100485-58-3

1-tetralone oxime

1-acetamidonaphthalene
575-36-0

1-acetamidonaphthalene

1-amino-naphthalene
134-32-7

1-amino-naphthalene

Conditions
Conditions Yield
With hydrogenchloride; acetic anhydride; acetic acid;

575-36-0 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 67-56-1
    67-56-1

    methanol

  • 60-29-7
    60-29-7

    diethyl ether

  • 35190-06-8
    35190-06-8

    1-(diacetylamino)naphthalene

575-36-0 Downstream products

  • 91394-66-0
    91394-66-0

    1-(acetylamino)-4-bromonaphthalene

  • 575-25-7
    575-25-7

    (3-fluoro-phenyl)-naphthalen-1-yl-amine

  • 93654-48-9
    93654-48-9

    N -[4-(4-nitro-phenylazo)-[1]naphthyl]-acetamide

  • 605-62-9
    605-62-9

    4-nitro-1-naphthol

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