6329-24-4

Basic information

• Product Name: N-(1-cyanonaphthalen-2-yl)acetamide
• Synonyms: acetamide, N-(1-cyano-2-naphthalenyl)-; N-(1-Cyano-2-naphthyl)acetamide
• CAS NO: 6329-24-4
• Molecular Formula: C₁₃H₁₀N₂O
• Molecular Weight: 210.2313
• Mol File: 6329-24-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 486.7°C at 760 mmHg
• Flash Point: 248.1°C
• Density: 1.22g/cm³
• Vapor Pressure: 1.27E-09mmHg at 25°C
• Refractive Index: 1.641
• CAS DataBase Reference: N-(1-cyanonaphthalen-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-cyanonaphthalen-2-yl)acetamide(6329-24-4)
• EPA Substance Registry System: N-(1-cyanonaphthalen-2-yl)acetamide(6329-24-4)

Safety Data

• Hazardous Substances Data: 6329-24-4(Hazardous Substances Data)

Usage

General Description

N-(1-Cyanonaphthalen-2-yl)acetamide is a chemical compound with the molecular formula C14H11NO. It is a derivative of naphthalene and is synthesized through the reaction of 2-naphthoyl chloride with hydroxylamine. N-(1-Cyanonaphthalen-2-yl)acetamide is commonly used in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceuticals and bioactive molecules. It has also been studied for its potential applications in the field of materials science, particularly in the development of organic semiconductors and electronic devices. N-(1-Cyanonaphthalen-2-yl)acetamide is a versatile compound with interesting properties, making it a valuable tool for researchers in a variety of fields.

Upstream product

• 79894-39-6 2-ethoxycarbonylaminonaphthalene-1-carbonitrile 
• 7066-13-9 2-aminonaphthalene-1-carbonitrile 
• 7597-73-1 N-(1-bromonaphthalen-2-yl)acetamide 
• 108-24-7 acetic anhydride 

Downstream Products

• 101874-56-0 2-benzylidenamino-[1]naphthonitrile 
• 103796-56-1 (+/-)-2t-amino-1,2,3,4-tetrahydro-[1r]naphthoic acid 
• 103796-56-1 (+/-)-2c-amino-1,2,3,4-tetrahydro-[1r]naphthoic acid 

Relevant articles and documents

STUDIES ON AROMATIC NITRO COMPOUNDS. II. REACTION OF 2-NITRONAPHTHALENE WITH MALONONITRILE IN THE PRESENCE OF BASES

Treatment of 2-nitronaphthalene with malononitrile and potassium hydroxide gave the potassium salt (II) of 1,1-dicyano-2-hydroxy-2-(1-cyano-2-naphthylamino)ethylene (II') in 78percent yield.II was hydrolyzed to 2-aminonaphthalene via 3-dicyanomethylene-3,4-dihydro-1H-naphthoxazin-1-one (III) when heated with 20percent hydrochloric acid.III reacted with amines to form benzoquinazolines (IVa-d).II was treated with hydrochloric acid in pyridine to yield the pyridinium salt (IIa) of II', and IIa was converted to II by treatment with potassium acetate.II was also synthesized from ethyl N-(1-cyano-2-naphthyl)carbamate, malononitrile and potassium amide.Keywords: 2-nitronaphthalene; malononitrile; 1,1-dicyano-2-hydroxy-2-(1-cyano-2-naphthylamino)ethylene; hydrolysis; potassium hydroxide; 2-substituted 1,3-dioxo-1,2,3,4-tetrahydrobenzoquinazolines; acylation; ethyl N-(1-cyano-2-naphthyl)-carbamate