723-42-2

Basic information

• Product Name: Ditolamide
• Synonyms: Ditolamide;4-Methyl-N,N-dipropylbenzenesulfonamide;N,N-Dipropyl-p-toluenesulfonamide;4-Methyl-N,N-di-n-propylbenzenesulfonaMide, 97%
• CAS NO: 723-42-2
• Molecular Formula: C₁₃H₂₁NO₂S
• Molecular Weight: 255.38
• Mol File: 723-42-2.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 358.6°C at 760 mmHg
• Flash Point: 170.7°C
• Appearance: /
• Density: 1.076g/cm³
• Vapor Pressure: 2.52E-05mmHg at 25°C
• Refractive Index: 1.517
• CAS DataBase Reference: Ditolamide(CAS DataBase Reference)
• NIST Chemistry Reference: Ditolamide(723-42-2)
• EPA Substance Registry System: Ditolamide(723-42-2)

Safety Data

• Hazardous Substances Data: 723-42-2(Hazardous Substances Data)

Usage

Description

Ditolamide is a chemical compound that serves as a plasticizer for specific types of polymers, such as imidazolidinetrione derivative polymers and polyparabanic acids. Its unique properties allow it to enhance the flexibility and processability of these polymers, making it a valuable additive in the manufacturing of various products.

Uses

Used in Plastics and Polymer Industry:
Ditolamide is used as a plasticizer for imidazolidinetrione derivative polymers, such as polyiminoimidazolinediones or polyparabanic acids, to improve their flexibility and processability. This enhancement allows for the creation of products with better performance characteristics and increased durability.

InChI:InChI=1/C13H21NO2S/c1-4-10-14(11-5-2)17(15,16)13-8-6-12(3)7-9-13/h6-9H,4-5,10-11H2,1-3H3

Upstream product

• 70-55-3 toluene-4-sulfonamide 
• 106-94-5 propyl bromide 
• 142-84-7 di-n-propylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 79-03-8 propionyl chloride 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 941-55-9 4-toluenesulfonyl azide 
• 102-69-2 tri-n-propylamine 
• 5775-34-8 N,N-Dipropyl-chloramine 
• 459-44-9 4-methylbenzenediazonium tetrafluoroborate 
• 1184-58-3 dimethylaluminum chloride 
• 57-66-9 4-[(dipropylamino)sulfonyl]benzoic acid 
• 74-88-4 methyl iodide 
• 74-85-1 ethene 

Relevant articles and documents

Debenzylative Sulfonylation of Tertiary Benzylamines Promoted by Visible Light

An efficient, general, inexpensive, and environmentally friendly photosynthesis of sulfonamides via visible light promoted debenzylative sulfonylation of tertiary benzylamines is described. Compared to the traditional S?N coupling reactions, which are promoted by oxidative C?N bond cleavage of symmetrical tertiary alkylamines, this strategy provides a selective C?N bond cleavage protocol and avoids the use of transition-metal, explosive oxidants, and ligands.

Palladium-Catalyzed Methylation of Aryl, Heteroaryl, and Vinyl Boronate Esters

A method for the direct methylation of aryl, heteroaryl, and vinyl boronate esters is reported, involving the reaction of iodomethane with aryl-, heteroaryl-, and vinylboronate esters catalyzed by palladium and PtBu2Me. This transformation occurs with a remarkably broad scope and is suitable for late-stage derivatization of biologically active compounds via the boronate esters. The unique capabilities of this method are demonstrated by combining carbon-boron bond-forming reactions with palladium-catalyzed methylation in a tandem transformation.

Charge-Transfer Complex Promoted Regiospecific C?N Bond Cleavage of Vicinal Tertiary Diamines

A catalyst-free, charge-transfer complex promoted coupling of sulfonyl chlorides with vicinal tertiary diamines to generate sulfonamides is presented. Mechanistic studies showed that these reactions are proceeded via charge transfer of vicinal tertiary diamines to sulfonyl chlorides, forming the unstable sulfonyl quaternary ammonium like complexes which induced the regiospecific intramolecular C?N bond cleavage of vicinal tertiary diamines. (Figure presented.).