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1,8-NAPHTHALALDEHYDIC ACID

  • CAS No.: 5811-87-0
  • Purity: 99%
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Manufacturer Supply Best Quality 1,8-NAPHTHALALDEHYDIC ACID 5811-87-0 with Efficient Transportation

  • Molecular Formula: C12H8O3
  • Molecular Weight: 200.194
  • Appearance/Colour: cream powder 
  • Vapor Pressure: 1.46E-08mmHg at 25°C 
  • Melting Point: 160-167 °C 
  • Boiling Point: 441.2 °C at 760 mmHg 
  • PKA: 2?+-.0.10(Predicted) 
  • Flash Point: 234.8 °C 
  • PSA: 54.37000 
  • Density: 1.354 g/cm3 
  • LogP: 2.35050 

1,8-NAPHTHALALDEHYDIC ACID(Cas 5811-87-0) Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 35, p. 823, 1992 DOI: 10.1021/jm00083a005

InChI:InChI=1/C12H8O3/c13-7-9-5-1-3-8-4-2-6-10(11(8)9)12(14)15/h1-7H,(H,14,15)/p-1

5811-87-0 Relevant articles

Organocatalytic, enantioselective intramolecular [6 + 2] cycloaddition reaction for the formation of tricyclopentanoids and insight on its mechanism from a computational study

Hayashi, Yujiro,Gotoh, Hiroaki,Honma, Masakazu,Sankar, Kuppusamy,Kumar, Indresh,Ishikawa, Hayato,Konno, Kohzo,Yui, Hiroharu,Tsuzuki, Seiji,Uchimaru, Tadafumi

supporting information; experimental part, p. 20175 - 20185 (2012/01/31)

Diphenylprolinol silyl ether was found t...

Ring-chain tautomerism. Part 10 +. The reaction of oxocarboxylic acids with diazodiphenylmethane

Bowden, Keith,Misic-Vukovic, Milica M.,Ranson, Richard J.

, p. 1601 - 1606 (2007/10/03)

The rate coefficients for the esterifica...

Reactions of carbonyl compounds in basic solutions. Part 28. The alkaline hydrolysis of 2-formylbenzonitrile, N-(2-formyl and -acetylphenyl)acetamides, N-(2-formylphenyl)-substituted benzamides, 4-(2-formylbenzoyl)morpholine, 3-(4-morpholino)- and -(N-methylanilino)-phthalides and -na

Bowden, Keith,Hiscocks, Simon P.,Reddy, M. Komal

, p. 1133 - 1138 (2007/10/03)

Rate coefficients have been measured for...

Formal transfers of hydride from carbon-hydrogen bonds. Attempted generation of H2 by intramolecular protonolyses of the activated carbon-hydrogen bonds of dihydrobenzimidazoles

Brunet,Wuest

, p. 689 - 696 (2007/10/03)

Protonolyses of carbon-hydrogen bonds ca...

5811-87-0 Process route

acenaphthene quinone
82-86-0

acenaphthene quinone

1,8-naphthalaldehydic acid
5811-87-0

1,8-naphthalaldehydic acid

Conditions
Conditions Yield
With potassium hydroxide; at 140 ℃; for 0.333333h;
68%
With potassium hydroxide; at 140 - 150 ℃;
acenaphthene quinone; With potassium hydroxide; In water; at 150 ℃; for 0.25h; Inert atmosphere;
With hydrogenchloride; water; Inert atmosphere;
3-Morpholin-4-yl-3H-benzo[de]isochromen-1-one

3-Morpholin-4-yl-3H-benzo[de]isochromen-1-one

morpholine
110-91-8,99108-56-2

morpholine

1,8-naphthalaldehydic acid
5811-87-0

1,8-naphthalaldehydic acid

Conditions
Conditions Yield
With water; hydroxide; In 1,4-dioxane; at 30 ℃; Thermodynamic data; Rate constant; ΔH(excit.), ΔS(excit.);
With water; hydroxide; In 1,4-dioxane; at 25 ℃; Rate constant;
With water; hydroxide; In 1,4-dioxane; at 35 ℃; Rate constant;
With water; hydroxide; In 1,4-dioxane; at 40 ℃; Rate constant;
With water; hydroxide; In 1,4-dioxane; at 25 - 40 ℃; Kinetics;

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