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2-Naphthaldehyde

  • CAS:66-99-9
  • MF:C11H8O
  • Purity:99%
  • Molecular Weight:156.184
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Product Details

  • CAS: 66-99-9
  • MF: C11H8O
  • Appearance: Pink crystalline
  • Offer Chemical Raw Material 2-Naphthaldehyde 66-99-9 In Stock

    • Molecular Formula:C11H8O
    • Molecular Weight:156.184
    • Appearance/Colour:Pink crystalline 
    • Vapor Pressure:0.00119mmHg at 25°C 
    • Melting Point:58-61 °C(lit.) 
    • Refractive Index:1.675 
    • Boiling Point:299.5 °C at 760 mmHg 
    • Flash Point:179.5 °C 
    • PSA:17.07000 
    • Density:1.155 g/cm3 
    • LogP:2.65230 

    2-Naphthaldehyde(Cas 66-99-9) Usage

    Synthesis Reference(s)

    Synthesis, p. 470, 1996 DOI: 10.1055/s-1996-4246

    Purification Methods

    Distil 2-naphthaldehyde with steam then crystallise it from water or EtOH. [Beilstein 7 IV 1288.]

    Definition

    ChEBI: A naphthaldehyde that is naphthalene substituted by a formyl group at position 2.

    InChI:InChI=1/C11H8O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-8H

    66-99-9 Relevant articles

    Effect of Mo loading on 2-naphthaldehyde formation from vapor phase oxidation of 2-methylnaphthalene with V2O5/TiO2 catalysts

    Gao, Xiaoqiang,Zhang, Fang,Yu, Yi,Dou, Yonghui,Xu, Li,Liu, Guoji

    , p. 47 - 51 (2019)

    Mo-modified V2O5/TiO2 catalysts were pre...

    Aerobic oxidation of alcohols enabled by nitrogen-doped copper nanoparticle catalysts

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    , p. 1043 - 1048 (2022/03/02)

    Heterogeneous nitrogen-doped carbon-inca...

    Controlled reduction of activated primary and secondary amides into aldehydes with diisobutylaluminum hydride

    Azeez, Sadaf,Kandasamy, Jeyakumar,Sabiah, Shahulhameed,Sureshbabu, Popuri

    supporting information, p. 2048 - 2053 (2022/03/31)

    A practical method is disclosed for the ...

    Selective functionalization of benzylic C-H bonds of two different benzylic ethers by bowl-shaped N -hydroxyimide derivatives as efficient organoradical catalysts

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    supporting information, p. 1021 - 1024 (2022/02/01)

    A highly efficient, site-selective benzy...

    Highly atom efficient synthesis of 2,2,4,5-tetrasubstituted 3(2H)-furanones having both hydroxyl and amino substituents

    Antony, Jesna,Mathai, Sindhu,Natarajan, Rakesh,P. Musthafa, Sumi,Rappai, John P.,S. Devaky, Karakkattu

    supporting information, (2022/02/25)

    We have developed a highly atom efficien...

    66-99-9 Process route

    17β-acetoxyandrost-2-en-3-yl 2-naphthoate

    17β-acetoxyandrost-2-en-3-yl 2-naphthoate

    stanolone acetate
    1164-91-6

    stanolone acetate

    (5α,17β)-3-oxoandrost-1-en-17-yl acetate
    64-82-4,6656-41-3,21507-42-6,25615-33-2,54631-35-5,79732-37-9,97413-69-9

    (5α,17β)-3-oxoandrost-1-en-17-yl acetate

    β-naphthaldehyde
    66-99-9

    β-naphthaldehyde

    Acetic acid (5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-2-(naphthalene-2-carbonyl)-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl ester
    65311-57-1

    Acetic acid (5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-2-(naphthalene-2-carbonyl)-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl ester

    Conditions
    Conditions Yield
    In hexane; at 0 ℃; Quantum yield; Mechanism; Product distribution; Irradiation; variation of wavelenght, concentration, solvent, irradiation intensity, reaction time;
    In cyclohexane; for 2h; Irradiation;
    15 mg
    30 mg
    25 mg
    250 mg
    5-(2-Naphthoyl)-5H-benzo<b>carbazole
    22013-66-7

    5-(2-Naphthoyl)-5H-benzocarbazole

    2,3-benzocarbazole
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    2,3-benzocarbazole

    β-naphthaldehyde
    66-99-9

    β-naphthaldehyde

    6-(2-Naphthoyl)benzo<b>carbazole
    78957-25-2

    6-(2-Naphthoyl)benzocarbazole

    Conditions
    Conditions Yield
    In cyclohexane; at 20 ℃; for 8h; Irradiation;
    3.5 % Chromat.
    1 % Chromat.
    0.7%

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