25267-41-8

Basic information

• Product Name: 2-Propenamide, N-(1,1-dimethylethyl)-, homopolymer 2-Propenamide,N-(1,1-dimethylethyl)-,homopolymer
• Synonyms: 2-Propenamide, N-(1,1-dimethylethyl)-, homopolymer 2-Propenamide,N-(1,1-dimethylethyl)-,homopolymer
• CAS NO: 25267-41-8
• Molecular Formula: C7H13NO
• Molecular Weight: 127.19
• Mol File: 25267-41-8.mol
• Article Data: 40

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propenamide, N-(1,1-dimethylethyl)-, homopolymer 2-Propenamide,N-(1,1-dimethylethyl)-,homopolymer(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenamide, N-(1,1-dimethylethyl)-, homopolymer 2-Propenamide,N-(1,1-dimethylethyl)-,homopolymer(25267-41-8)
• EPA Substance Registry System: 2-Propenamide, N-(1,1-dimethylethyl)-, homopolymer 2-Propenamide,N-(1,1-dimethylethyl)-,homopolymer(25267-41-8)

Safety Data

• Hazardous Substances Data: 25267-41-8(Hazardous Substances Data)

Usage

Main properties

Colorless
Odorless
Soluble in water
High melting point
Excellent adhesive properties
High tensile strength
Resistance to chemicals and heat
Improves physical properties of materials
Compatible with other substances

Specific content

Polymer compound formed from the homopolymerization of 2-Propenamide, N-(1,1-dimethylethyl)-
Used in adhesives, coatings, and encapsulation agents
Valuable in various industries for its versatility and properties

Upstream product

• 107-13-1 acrylonitrile 
• 75-65-0 tert-butyl alcohol 
• 7664-93-9 sulfuric acid 
• 92-84-2 10H-phenothiazine 
• 115-11-7 isobutene 
• 24424-99-5 di-tert-butyl dicarbonate 
• 56-87-1 L-lysine 
• 540-88-5 acetic acid tert-butyl ester 
• 107-12-0 propiononitrile 
• 75-64-9 tert-butylamine 
• 74-86-2 acetylene 
• 732-26-3 2,4,6-tri-tert-butylphenoxol 
• 99065-81-3 2-acetoxy-propionic acid tert-butylamide 
• 15214-89-8 2-acrylamido-2-methylpropanesulfonic acid 

Downstream Products

• 1622221-54-8 (E)-N-(tert-butyl)-3-tosylacrylamide 
• 1579941-80-2 (E)-2-(2-(3-(tert-butylamino)-3-oxoprop-1-enyl)-4-methylthiazol-5-yl)ethyl benzoate 
• 1118-32-7 N-tert-butylpropionamide 
• 7064-25-7 6.6-Dimethyl-N-t.-butyl-pyrrolo<1.2-b>isoxazol-2-carbonsaeure-amid 
• 619-73-8 4-nitrobenzyl chloride 
• 62-23-7 4-nitro-benzoic acid 

Relevant articles and documents

Reactivity of secondary N-alkyl acrylamides in Morita–Baylis–Hillman reactions

The Morita–Baylis–Hillman (MBH) reaction of secondary N-alkyl acrylamides, discarded up to now from investigations of the scope of activated alkenes, was studied. Optimization of the reaction conditions revealed that a balance must be found between activation of the MBH coupling reaction and that of the undesired competitive aldehyde Cannizzaro reaction. Using 3-Hydroxyquinuclidine (3-HQD) in a 1:1 water-2-MeTHF mixture provides the appropriate conditions that were applicable to a wide range of diversely substituted secondary N-alkyl acrylamides and aromatic aldehydes, giving rise to novel amide-containing MBH adducts under mild and clean conditions.

A convenient synthesis of N-tert-butyl amides by the reaction of di-tert-butyl dicarbonate and nitriles catalyzed by Cu(OTf)2

The utility of Cu(OTf)2 as the catalyst for the synthesis of a series of N-tert-butyl amides in excellent isolated yields via the reaction of nitriles (alkyl, aryl, benzyl, and furyl nitriles) with di-tert-butyl dicarbonate is described. Cu(OTf)2 is a highly stable and efficient catalyst for the present Ritter reaction under solvent-free conditions at room temperature.

CoFe2O4?SiO2-NH-βCD-BF3 as a supramolecular nanocomposite: Synthesis, characterization and catalytic activity

This manuscript describes synthesis of BF3-functionlized β-cylcodextrine grafted magnetic CoFe2O4 nanaoparticles as a hybrid magnetic nano-composite (CoFe2O4?SiO2-NH-βCD-BF3). The CoFe2O4?SiO2-NH-βCD-BF3 was fabricated by grafting of 6-O-toluenesulfonyl cyclodextrin (6-Ts-βCD) to 3-aminopropyl triethoxysilane coated magnetic CoFe2O4?SiO2 nanoparticles followed by combination with BF3. The CoFe2O4?SiO2-NH-βCD-BF3was characterized by FT-IR, TGA, VSM and SEM techniques. The feasibility of using CoFe2O4?SiO2-NH-βCD-BF3 as a magnetically recoverable catalyst was confirmed in the modified-Ritter reaction. The result showed that this novel nano-composite could serve as an efficient nanoreactor bearing super-acidic sites formed by immobilized BF3 and reuse at least for 6 times without loss in activity.