ChemicalBook--->CAS DataBase List--->23204-36-6

23204-36-6

23204-36-6 Structure

23204-36-6 Structure
IdentificationBack Directory
[Name]

3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE
[CAS]

23204-36-6
[Synonyms]

Albb-005281
hydroxynaphthalicanhydride
3-Hydroxynaphthalic anhydride
3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE
5-HYDROXY-BENZO[DE]ISOCHROMENE-1,3-DIONE
5-hydroxy-1H,3H-benzo[de]isochromene-1,3-dione
3-Hydroxy-1,8-naphthalenedicarboxylic anhydride
3-Hydroxynaphthalene-1,8-dicarboxylic anhydride
3-Hydroxy-1,8-naphthalenedicarboxylic acid=anhydride ester
[Molecular Formula]

C12H6O4
[MDL Number]

MFCD00059759
[MOL File]

23204-36-6.mol
[Molecular Weight]

214.17
Chemical PropertiesBack Directory
[Melting point ]

281 °C
[Boiling point ]

509.4±33.0 °C(Predicted)
[density ]

1.585±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

soluble in Dimethylformamide
[form ]

powder to crystal
[pka]

7.93±0.20(Predicted)
[color ]

Light yellow to Yellow
[InChI]

InChI=1S/C12H6O4/c13-7-4-6-2-1-3-8-10(6)9(5-7)12(15)16-11(8)14/h1-5,13H
[InChIKey]

FKVNZFAMXGMPOU-UHFFFAOYSA-N
[SMILES]

C1(=O)OC(=O)C2=CC(O)=CC3=C2C1=CC=C3
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

2917.39.7000
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Uses]

Used as pharmaceutical intermediates for RD.
[Synthesis]

5-AMINO-BENZO[DE]ISOCHROMENE-1,3-DIONE

23204-38-8

3-Hydroxy-1,8-naphthalic anhydride

23204-36-6

General procedure for the synthesis of 5-hydroxybenzo[de]isochroman-1,3-dione from 5-amino-1H,3H-benzo[DE]isochroman-1,3-dione: Compound 3 (8 mmol, 1.7 g) was placed in a three-necked flask, and 432 mL of aqueous sulfuric acid solution (sulfuric acid to water in a ratio of 1:5, by volume) was added and the reaction system was cooled down to 0 °C. Subsequently, sodium nitrite (12 mmol, 0.81 g) was slowly added and stirred continuously at 0 °C for 1 hour. After completion of the reaction, the reaction system was gradually warmed to room temperature and then stirred at 120 °C for 12 hours. At the end of the reaction, the reaction mixture was cooled to room temperature, filtered through a Kiriyama funnel and the filter cake was washed with water and dried. The crude product was recrystallized with chloroform to afford the target product 5-hydroxybenzo[de]isochromene-1,3-dione.

[References]

[1] Patent: JP2018/39777, 2018, A. Location in patent: Paragraph 0115; 0119; 0120
[2] Journal of Photochemistry and Photobiology A: Chemistry, 2015, vol. 303-304, p. 28 - 35
Spectrum DetailBack Directory
[Spectrum Detail]

3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE(23204-36-6)MS
3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE(23204-36-6)1HNMR
3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE(23204-36-6)13CNMR
3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE(23204-36-6)IR1
3-HYDROXY-1,8-NAPHTHALIC ANHYDRIDE(23204-36-6)IR2
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