4-AMINO-1,8-NAPHTHALIC ANHYDRIDE

Product Information

Molecular Formula:
C12H8N2O2
Molecular Weight:
212.20
Description
4-AMINO-1,8-NAPHTHALIC ANHYDRIDE is a key component in the synthesis of various pharmaceuticals and dyes. With its aromatic structure, it finds applications in the development of drugs targeting cancer and autoimmune diseases. Its versatility also extends to the creation of dyes used in industries such as textiles and electronics.
Synonyms
6-AMINO-BENZO[DE]ISOQUINOLINE-1,3-DIONE; 4-AMINO-1,8-NAPHTHALIC ANHYDRIDE; 4-AMINO-1,8-NAPHTHALIMIDE; 4-ANI; TIMTEC-BB SBB000529; TIMTEC-BB SBB003425; 4-aminonaphthalene-1,8-dicarboxylic anhydride; 6-Aminobenz[de]isochromene-1,3-dione
IUPAC Name
8-amino-3-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8,10-pentaene-2,4-dione
Canonical SMILES
C1=CC2=C(C=CC3=C2C(=C1)C(=O)OC3=O)N
InChI
InChI=1S/C12H7NO3/c13-9-5-4-8-10-6(9)2-1-3-7(10)11(14)16-12(8)15/h1-5H,13H2
InChI Key
QIXHMCMCFSNKOG-UHFFFAOYSA-N
Purity
0.95
Density
1.105 g/mL at 25 °C(lit.)

Safety Information

Hazards
H302 + H312 + H332 - H315 - H319 - H335 - H350
Precautionary Statement
P201 - P280 - P301 + P312 + P330 - P302 + P352 + P312 - P304 + P340 + P312 - P308 + P313

Computed Properties

XLogP3
1.9
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
0
Exact Mass
213.042593085 g/mol
Monoisotopic Mass
213.042593085 g/mol
Topological Polar Surface Area
69.4Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
341
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113354584-A Naphthalimide fluorescent probe for distinguishing Cys, Hcy and GSH, and preparation method and application thereof 2021-06-15
CN-112521738-A Degradable light conversion film and preparation method and application thereof 2020-12-16
CN-112521738-B Degradable light conversion film and preparation method and application thereof 2020-12-16
WO-2021231998-A1 High-temperature, thermally-insulative laminates including aerogel layers 2020-05-15
WO-2021232001-A1 Low-dielectric constant, low-dissipation factor laminates including aerogel layers 2020-05-15
WO-2021217073-A2 Air permeable filter material comprising a polymer aerogel 2020-04-24
WO-2020198264-A1 Modified cleavases, uses thereof and related kits 2019-03-26
US-2021214701-A1 Modified cleavases, uses thereof and related kits 2019-03-26
CA-3134776-A1 Modified cleavases, uses thereof and related kits 2019-03-26
CN-113993997-A Modified cleaving enzymes, uses thereof and related kits 2019-03-26

Literatures

PMID Publication Date Title Journal
17070119 2007-03-01 Assessment of 4-nitro-1,8-naphthalic anhydride reductase activity in homogenates of bakers' yeast by reversed-phase high-performance liquid chromatography Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
16851591 2005-03-30 Aminonaphthalic anhydrides as red-emitting materials: electroluminescence, crystal structure, and photophysical properties The journal of physical chemistry. B
5819 1975-10-17 [Clinical experiences with the Kö 1366 (Bunitrololhydrochloride) beta receptor blockader and the combination Kö 1366/Isosorbitdinitrate in patients with coronary disease] Wiener medizinische Wochenschrift (1946)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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