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
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, p. 689 - 696 (2007/10/03)
Protonolyses of carbon-hydrogen bonds ca...
5811-87-0 Process route
-
-
82-86-0
acenaphthene quinone
-
-
5811-87-0
1,8-naphthalaldehydic acid
| 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
-
-
110-91-8,99108-56-2
morpholine
-
-
5811-87-0
1,8-naphthalaldehydic acid
| 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;
|
5811-87-0 Upstream products
-
465-99-6
hedaragenin
-
82-86-0
acenaphthene quinone
-
5656-90-6
8-formyl-1-naphthalenecarboxylic acid (lactol form)
-
83-32-9
acenaphthene
5811-87-0 Downstream products
-
30934-48-6
1,8-naphthaldehydic acid methyl ester
-
19310-98-6
8-methyl-1-naphthoic acid
-
5656-90-6
8-formyl-1-naphthalenecarboxylic acid (lactol form)
-
518-05-8
Naphthalene-1,8-dicarboxylic acid