7274-71-7

Basic information

• Product Name: N-(4-METHOXY-PHENYL)-2-METHYL-ACRYLAMIDE
• Synonyms: N-(4-METHOXY-PHENYL)-2-METHYL-ACRYLAMIDE;2-Propenamide, N-(4-methoxyphenyl)-2-methyl-;N-(4-Methoxy-Phenyl)-2-Methyl-Acrylamide(WXC04133)
• CAS NO: 7274-71-7
• Molecular Formula: C₁₁H₁₃NO₂
• Molecular Weight: 191.23
• Product Categories: pharmacetical
• Mol File: 7274-71-7.mol
• Article Data: 38

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-METHOXY-PHENYL)-2-METHYL-ACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-METHOXY-PHENYL)-2-METHYL-ACRYLAMIDE(7274-71-7)
• EPA Substance Registry System: N-(4-METHOXY-PHENYL)-2-METHYL-ACRYLAMIDE(7274-71-7)

Safety Data

• Hazardous Substances Data: 7274-71-7(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 80-62-6 methacrylic acid methyl ester 
• 920-46-7 Methacryloyl chloride 
• 760-93-0 methacryloyl anhydride 
• 1970-56-5 p-methoxy-α-bromoisobutyranilide 
• 7677-24-9 trimethylsilyl cyanide 
• 1242029-34-0 N-(4-methoxyphenyl)-N-(prop-2-yn-1-yl)methacrylamide 
• 51491-68-0 2-phenylacrylyl chloride 
• 79-41-4 poly(methacrylic acid) 
• 557-93-7 2-bromoprop-1-ene 
• 201230-82-2 carbon monoxide 

Downstream Products

• 126335-11-3 3-Chloro-2-ethylsulfanyl-N-(4-methoxy-phenyl)-2-methyl-propionamide 
• 87568-30-7 1-(p-methoxyphenyl)-3-methyl-3-(phenylthio)azetidin-2-one 
• 87568-26-1 3-Chloro-N-(4-methoxy-phenyl)-2-methyl-2-phenylsulfanyl-propionamide 
• 87568-28-3 2-Chloro-N-(4-methoxy-phenyl)-2-methyl-3-phenylsulfanyl-propionamide 
• 69193-56-2 1-(4-methoxyphenyl)-3-methylideneazetidin-2-one 
• 87568-43-2 1-(4'-methoxyphenyl)-azetidin-2,3-dione 
• 87568-44-3 1-(p-methoxyphenyl)azetidin-2-one 3-oxime 
• 87568-45-4 3-amino-1-(p-methoxyphenyl)azetidin-2-one 
• 87568-42-1 1-(p-methoxyphenyl)-3-methyl-3-(phenylsulfinyl)azetidin-2-one 
• 87568-46-5 3-(((benzyloxy)carbonyl)amino)-1-(p-methoxyphenyl)azetidin-2-one 
• 126335-19-1 Acetic acid 2-ethylsulfanyl-2-(4-methoxy-phenylcarbamoyl)-propyl ester 
• 294642-84-5 N-(4-methoxyphenyl)-N,2-dimethylacrylamide 
• 1256971-24-0 1-(4-methoxyphenyl)-3-methyl-5,6-diphenylpyridin-2(1H)-one 
• 1403475-23-9 C₁₈H₁₇Br₂NO₂ 

Relevant articles and documents

Substituent-induced delocalization effects on hydrogen-bonding interaction in poly(N-phenyl methacrylamide) derivatives

Within small molecules, the hydrogen-bonding behaviors affected by delocalization have been studied thoroughly, but rare publication in macromolecules. Therefore, three poly(N-phenyl methacrylamide)s, poly(N-phenyl methacrylamide) (PNPAA), poly(N-4-methox

Bromo Radical-Mediated Photoredox Aldehyde Decarbonylation towards Transition-Metal-Free Hydroalkylation of Acrylamides at Room Temperature

Herein, we report a visible-light-mediated hydroalkylation reaction of alkenes using easily available aldehydes as alkyl sources via bromo radical-promoted photoredox decarbonylation. This protocol provides an alternative entry to C(sp3)?C(sp3) bond formation and features considerable advantages including mild and clean reaction conditions, obviation for transition-metal catalyst, and good functional group compatibility.

Reactions of 2,3-Dibromo-2-methylpropanamides Promoted by Potassium tert-Butoxide

Abstract: 2,3-Dibromo-2-methylpropanamides with different substituents on the nitrogen atom were synthe-sized, and their transformations by the action of potassium tert-butoxide in THF were studied. 2,3-Dibromo-N-(4-methoxyphenyl)-2-methylpropanamide and 2,3-dibromo-N-(2,5-dibromo-4-methoxyphenyl)-2-methyl-propan-amide reacted with 1–2 equiv of t-BuOK to give the corresponding N-substituted 3-bromo-3-methyl- and 3-methylideneazetidin-2-ones with acceptable yields and selectivity. Increase of the amount of t-BuOK to 3–5 equiv led to significant reduction of the yield of vinyl bromides and 3-methylideneazetidin-2-ones. On the other hand, the reaction of 2,3-dibromo-N-(tert-butyl)-2-methylpropanamide with t-BuOK afforded 3-(tert-bu-toxymethyl)-1-tert-butylazetidin-2-one with a good yield and selectivity.