21911-75-1 Usage
General Description
N-phenyl-N-methylglycine hydrochloride is a chemical compound with the formula C9H12NO2. A hydrochloride salt of N-phenyl-N-methylglycine, it is an organic chemical substance, commonly used in laboratory environments and industrial manufacturing. N-phenyl-N-methylglycine hydrochloride exists as a stable salt, meaning that it can be safely stored for extended periods. N-phenyl-N-methylglycine hydrochloride serves a unique function as a part of various processes, such as a reagent in chemical reactions or a component in the creation of other chemical compounds. However, its specific use can vary widely depending on the context and the aims of the procedure or production method it's used in.
Check Digit Verification of cas no
The CAS Registry Mumber 21911-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,1 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21911-75:
(7*2)+(6*1)+(5*9)+(4*1)+(3*1)+(2*7)+(1*5)=91
91 % 10 = 1
So 21911-75-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-10(7-9(11)12)8-5-3-2-4-6-8/h2-6H,7H2,1H3,(H,11,12)
21911-75-1Relevant articles and documents
Iron-catalyzed reductive strecker reaction
Yan, Fachao,Huang, Zijun,Du, Chen-Xia,Bai, Jian-Fei,Li, Yuehui
, p. 188 - 194 (2021/02/03)
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.
Cycloadditions of (Arylalkylamino)ketenes with Cycloalkenes
Brady, William T.,Gu, Yi Qi
, p. 2834 - 2838 (2007/10/02)
(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
