42340-32-9

Basic information

• Product Name: 2-(4-METHOXYPHENYL)-1H-BENZ(de)ISO-QUINOLINE-1,3(2H)-DIONE
• Synonyms: 2-(4-methoxy-phenyl)-benzo[de]isoquinoline-1,3-dione;N-p-methoxyphenylnaphthalic imide
• CAS NO: 42340-32-9
• Molecular Formula: C19H13NO3
• Molecular Weight: 303.317
• Mol File: 42340-32-9.mol
• Article Data: 8

Chemical Properties

• Melting Point: 200 °C(Solv: ethanol (64-17-5))
• Boiling Point: 542.5±42.0 °C(Predicted)
• Density: 1.348±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-(4-METHOXYPHENYL)-1H-BENZ(de)ISO-QUINOLINE-1,3(2H)-DIONE (CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-METHOXYPHENYL)-1H-BENZ(de)ISO-QUINOLINE-1,3(2H)-DIONE (42340-32-9)
• EPA Substance Registry System: 2-(4-METHOXYPHENYL)-1H-BENZ(de)ISO-QUINOLINE-1,3(2H)-DIONE (42340-32-9)

Safety Data

• Safety Statements: A poison by intraperitoneal route. When heated to decomposition it emits toxic vapors of NOsub xmlns="">x/sub>.
• HazardClass: 3
• Hazardous Substances Data: 42340-32-9(Hazardous Substances Data)

Usage

General Description

The chemical "2-(4-METHOXYPHENYL)-1H-BENZ(de)ISO-QUINOLINE-1,3(2H)-DIONE" is a compound with a molecular structure that includes a benzisoquinoline core with a 1,3-dione functional group and a methoxyphenyl substituent. 2-(4-METHOXYPHENYL)-1H-BENZ(de)ISO-QUINOLINE-1,3(2H)-DIONE is often used in medicinal and pharmaceutical research due to its potential for biological activity and therapeutic properties. It may have applications in drug development, particularly in the treatment of various diseases, as it is believed to have potential pharmacological effects. Researchers and scientists continue to explore and study the properties and potential uses of this chemical for various applications in the field of medicine and pharmaceuticals.

Upstream product

• 81-84-5 1,8-Naphthalic anhydride 
• 104-94-9 4-methoxy-aniline 
• 2101-87-3 p-methoxy-phenylazide 

Downstream Products

• 6424-77-7 2,9-bis(4-methoxyphenyl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone 

Relevant articles and documents

Persistent Room-Temperature Radicals from Anionic Naphthalimides: Spin Pairing and Supramolecular Chemistry

N-Substituted naphthalimides (NNIs) have been shown to exhibit highly efficient and persistent room-temperature phosphorescence from an NNI-localized triplet excited state, when the N-substitution is a sufficiently strong donor and mediates an intramolecu

The new fluorescent naphthalic imide derivatives having the inductive ending group

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A "green" route to perylene dyes: Direct coupling reactions of 1,8-naphthalimide and related compounds under mild conditions using a "new" base complex reagent, t-BuOK/DBN

The direct coupling reactions of 1,8-naphthalimide compounds efficiently occurred at 130 or 170 °C without the intervention of the leuco form dyes in the presence of base complex reagent, t-BuOK/1,5-diazabicyclo[4.3.0]non-5-ene (DBN), to give the corresponding perylene dyes in good yields with >95% purities. A possible mechanistic speculation for these oxidative coupling reactions is briefly discussed.