36043-57-9

Basic information

• Product Name: N-DECYLPHTHALIMIDE
• Synonyms: N-DECYLPHTHALIMIDE
• CAS NO: 36043-57-9
• Molecular Formula: C₁₈H₂₅NO₂
• Molecular Weight: 287.4
• Mol File: 36043-57-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 397.5 °C at 760 mmHg
• Flash Point: 155.9 °C
• Appearance: /
• Density: 1.055 g/cm³
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: N-DECYLPHTHALIMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-DECYLPHTHALIMIDE(36043-57-9)
• EPA Substance Registry System: N-DECYLPHTHALIMIDE(36043-57-9)

Safety Data

• Hazardous Substances Data: 36043-57-9(Hazardous Substances Data)

Upstream product

• 2050-77-3 Iododecane 
• 1074-82-4 potassium phtalimide 
• 2016-57-1 1-aminodecane 
• 201230-82-2 carbon monoxide 
• 66-77-3 1-naphthaldehyde 
• 100-52-7 benzaldehyde 

Downstream Products

• 135382-81-9 N-Decyl-2-(pyrrolidine-1-carbonyl)-benzamide 
• 2016-57-1 1-aminodecane 
• 6300-55-6 2-decyl-2-methyl-isoindolinium; iodide 
• 1459737-08-6 (4-(decylcarbamoyl)phenyl)boronic acid 

Relevant articles and documents

Method for constructing N-(n-decyl)phthalimide in one step by using imine as starting material

The invention discloses a method for constructing N-(n-decyl)phthalimide in one step by using an imine as a starting material. (E)-N-n-decyl-1-phenylmethylimine used as a reaction raw material undergoes a carbonylation reaction to form the N-(n-decyl)phthalimide. The method has the characteristics of mild reaction conditions, simple operation process and excellent yield.

A method for utilizing the carbonylation reaction one-pot synthesis N - substituted phthalimide method

The invention relates to a one-pot method for synthesizing N-substituted phthalimide through carbonylation. The method comprises the following steps: adding aromatic aldehyde, amine, a metal palladium catalyst and a solvent into a reaction container, then adding a copper salt as an oxidizing agent and carrying out stirring for 4 to 24 h at normal temperature; sleeving the reaction container with a balloon filled with carbon monoxide and oxygen and carrying out a stirring reaction at 40 to 150 DEG C for 12 to 72 h; after completion of the reaction, carrying out cooling to room temperature and dismounting the balloon; subjecting a reaction solution to filtering and carrying out pressure reduced evaporation to remove a solvent so as to obtain a crude product; and subjecting the crude product to column chromatographic purification so as to obtain the N-substituted phthalimide. The one-pot method for synthesizing N-substituted phthalimide through carbonylation is simple and safe to operate, uses easily available and cheap raw materials, has good function group applicability and can be used for synthesis of a plurality of drug molecules; and the method has excellent yield, is favorable for industrial production and has important application values in organic synthesis.