38357-69-6

Basic information

• Product Name: 1-Naphthalenol,phenylcarbamate(9CI)
• Synonyms: 1-Naphthalenol,phenylcarbamate(9CI)
• CAS NO: 38357-69-6
• Molecular Formula: C₁₇H₁₃NO₂
• Molecular Weight: 0
• Product Categories: N-CBZ
• Mol File: 38357-69-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Naphthalenol,phenylcarbamate(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol,phenylcarbamate(9CI)(38357-69-6)
• EPA Substance Registry System: 1-Naphthalenol,phenylcarbamate(9CI)(38357-69-6)

Safety Data

• Hazardous Substances Data: 38357-69-6(Hazardous Substances Data)

Usage

Type

Organic compound

Use

Pesticide for controlling insects

Mechanism

Inhibits the activity of the enzyme acetylcholinesterase, which is essential for the proper functioning of the nervous system in insects

Effects

Leads to paralysis and ultimately death of the target insects

Applications

Used in a variety of agricultural, commercial, and residential settings, as well as in the production of animal feed and pet care products

Toxicity

Low toxicity to humans

Effectiveness

Controls a wide range of insect pests

Upstream product

• 90-15-3 α-naphthol 
• 103-71-9 phenyl isocyanate 
• 3759-61-3 1-naphthyl chloroformate 
• 62-53-3 aniline 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 108-86-1 bromobenzene 

Downstream Products

• 13545-65-8 1-hydroxynaphthalene-2-carboxanilide 
• 90-15-3 α-naphthol 
• 103-71-9 phenyl isocyanate 
• 101-68-8 di(4-isocyanatophenyl)methane 

Relevant articles and documents

A Fe3O4?SiO2/Schiff Base/Pd Complex as an Efficient Heterogeneous and Recyclable Nanocatalyst for One-Pot Domino Synthesis of Carbamates and Unsymmetrical Ureas

A palladium-catalyzed domino method for the direct synthesis of carbamates and ureas has been developed by using readily available and economical starting materials (aryl halide, carbon monoxide, sodium azide, amines and alcohols) in a one-pot approach. The domino process underwent carbonylation, Curtius rearrangement, and nucleophilic addition. This protocol provides a step-economical and highly efficient reaction to access the wide range of valuable carbamates, symmetrical and unsymmetrical ureas with high yields under remarkable mild reaction conditions that are important factors in pharmaceutical science, biochemistry and agricultural industries. Furthermore, the magnetically recoverable nanocatalyst (Fe3O4?SiO2/Pd(II)) can be conveniently and swiftly recycled using external magnet and reused at least for seven times without noticeable loss of its catalytic activity.