116507-58-5 Usage
Uses
Used in Pharmaceutical Industry:
(2S,3R)-Methyl 3-((methoxycarbonyl)amino)-2-methyl-3-phenylpropanoate is used as a key building block for the synthesis of various pharmaceuticals and organic compounds. Its unique chiral structure allows for the creation of enantiomerically pure compounds, which are essential in the development of effective and safe medications.
Used in Research and Development:
(2S,3R)-Methyl 3-((methoxycarbonyl)amino)-2-methyl-3-phenylpropanoate is also utilized in research and development settings to explore its potential applications and properties. Scientists and chemists investigate its reactivity, stability, and interactions with other molecules to enhance understanding and facilitate the design of new chemical entities.
Safety Note:
It is important to handle (2S,3R)-Methyl 3-((methoxycarbonyl)amino)-2-methyl-3-phenylpropanoate with care, as it may pose hazards if improperly managed or inhaled. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 116507-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116507-58:
(8*1)+(7*1)+(6*6)+(5*5)+(4*0)+(3*7)+(2*5)+(1*8)=115
115 % 10 = 5
So 116507-58-5 is a valid CAS Registry Number.
116507-58-5Relevant academic research and scientific papers
Carbamate-Directed Stereoselective Hydrogenation and Kinetic Resolution of N-Protected α-(α-Aminoalkyl)acrylates
Takagi, Masatoshi,Yamamoto, Keiji
, p. 8869 - 8882 (2007/10/02)
A series of racemic methyl α-acrylates (1a-e) were hydrogenated using a variety of Rh(I) cationic complexes containing diphosphines and a chiral (BINAP = 2,2'-bis(diphenylphosphino)-1,1'-dinaphthyl) as ca
Diastereoselective Hydrogenation of Methyl 2-acrylate Catalyzed by Ru(II) or Rh(I) Complexes
Yamamoto, Keiji,Takagi, Masatoshi,Tsuji, Jiro
, p. 319 - 321 (2007/10/02)
The title compound was prepared and hydrogenated by using a Ru(II)- or Rh(I)-phosphine catalyst precursor with excellent anti-selectivity, the results indicating that a ligating group, NHCO2Me, may direct the addition of hydrogen to an olefinic diastereof
