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2-Naphthaldehyde

  • Product Name: 2-Naphthaldehyde
  • CAS: 66-99-9
  • Purity:
  • Appearance: Pink crystalline

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Factory supply good quality 2-Naphthaldehyde 66-99-9 with 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

Kobayashi, Shū,Tobita, Fumiya,Yamashita, Yasuhiro,Yasukawa, Tomohiro

, 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 ...

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...

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

Kato, Terumasa,Maruoka, Keiji

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

A highly efficient, site-selective benzy...

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
243-28-7

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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