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2-Naphthaldehyde

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

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Product Details

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

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stanolone acetate

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

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β-naphthaldehyde

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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

: 22013-66-7
5-(2-Naphthoyl)-5H-benzocarbazole

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2,3-benzocarbazole

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β-naphthaldehyde

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6-(2-Naphthoyl)benzocarbazole

Conditions

Conditions Yield

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

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

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