21911-75-1

Usage

Uses

Used in Chemical Synthesis:
N-phenyl-N-methylglycine hydrochloride is used as a reagent for facilitating chemical reactions, contributing to the synthesis of a wide range of chemical compounds. Its role in these processes is crucial for achieving the desired outcomes in the production of various substances.
Used in Laboratory Research:
In the context of scientific research, N-phenyl-N-methylglycine hydrochloride is used as a component in experimental setups. It aids in the exploration of chemical properties and reactions, furthering our understanding of chemical processes and their applications.
Used in Industrial Manufacturing:
N-phenyl-N-methylglycine hydrochloride is employed in industrial applications as a key component in the production of various products. Its stability and reactivity make it a valuable asset in the manufacturing of chemicals and other materials, enhancing the efficiency and effectiveness of industrial processes.

InChI:InChI=1/C9H11NO2/c1-10(7-9(11)12)8-5-3-2-4-6-8/h2-6H,7H2,1H3,(H,11,12)

Upstream product

• 107-97-1 sarcosine 
• 21911-74-0 (methyl-phenyl-amino)-acetic acid ethyl ester 
• 36602-08-1 (N-methylanilino)acetonitrile 
• 93-61-8 N-methyl-N-phenylformamide 
• 20059-60-3 N-methyl-N-p-phenylglycine methyl ester 

Downstream Products

• 120638-47-3 cis-1-(p-methoxyphenyl)-3-(methylphenylamino)-4-(p-nitrophenyl)-2-azetidinone 
• 120547-18-4 endo-10-(methylphenylamino)bicyclo<6.2.0>decan-9-one 
• 120638-36-0 cis-1-phenyl-3-(methylphenylamino)-4-(2-phenylethenyl)-2-azetidinone 
• 120638-48-4 cis-1-phenyl-3-(methylphenylamino)-4-(o-methoxyphenyl)-2-azetidinone 
• 120638-52-0 trans-1-phenyl-3-(methylphenylamino)-4-(o-methoxyphenyl)-2-azetidinone 
• 135569-40-3 cis-1-benzyl-3-(methylphenylamino)-4-(p-methoxyphenyl)-2-azetidinone 
• 120638-43-9 cis-1,4-bis(p-methoxyphenyl)-3-(methylphenylamino)-2-azetidinone 
• 135569-39-0 trans-1-(o-methylphenyl)-3-(methylphenylamino)-4-phenyl-2-azetidinone 
• 135569-46-9 trans-1-(2,6-dimethylphenyl)-3-(methylphenylamino)-4-(p-nitrophenyl)-2-azetidinone 
• 135569-41-4 cis-1-benzyl-3-(methylphenylamino)-4-(o-methoxyphenyl)-2-azetidinone 
• 135569-37-8 cis-1-benzyl-3-(methylphenylamino)-4-phenyl-2-azetidinone 
• 135569-48-1 cis-1-(p-methoxyphenyl)-3-(methylphenylamino)-4-(α-naphthyl)-2-azetidinone 
• 135569-45-8 trans-1-(2,6-dimethylphenyl)-3-(methylphenylamino)-4-(p-chlorophenyl)-2-azetidinone 
• 135569-43-6 trans-1-α-naphthyl-3-(methylphenylamino)-4-(p-chlorophenyl)-2-azetidinone 

Relevant academic research and scientific papers

Iron-catalyzed reductive strecker reaction

Strecker reaction is widely applied for the synthesis of amino acids from aldehydes, amines and cyanides. Herein, we report the FeI2-catalyzed reductive Strecker type reaction of formamides instead of aldehydes to produce amino acetonitriles. The challenging capture of carbinolamine intermediates by CN? was achieved via Fe catalysis. This approach afforded better yields than the use of Ir- or Rh-catalysts. The application ability of this methodology is demonstrated by 1) one-pot construction of (13C labeled) complex molecules from CO2 via amino acetonitrile intermediates and 2) convenient production of homologated carboxylic acids from aldehydes.

Amide derivatives and methods of their use

Amide derivatives of the general formulae Ia and Ib: are disclosed. Pharmaceutical compositions containing these compounds, and methods for their use, inter alia, for treating and/or preventing gastrointestinal disorders, pain, and pruritus are also disclosed.

Cycloadditions of (Arylalkylamino)ketenes with Cycloalkenes

(Arylalkylamino)ketenes were prepared from the corresponding glycine derivatives and underwent in situ cycloadditions with cyclopentadiene, cycloheptene, and cyclooctene to yield only the endo-bicyclocyclobutanones.The cycloheptene and cyclooctene cycload