13088-92-1 Usage
Uses
Used in Pharmaceutical Industry:
[S,(-)]-α-Ethyl-α-methylbenzylamine is used as a chiral auxiliary for the synthesis of enantiomerically pure compounds. Its application is crucial in creating drugs with specific desired effects, as the compound's chiral nature allows for the control of stereochemistry in reactions.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, [S,(-)]-α-Ethyl-α-methylbenzylamine serves as a chiral auxiliary and ligand in asymmetric catalysis. This enables the production of enantiomerically pure agrochemicals, which can be more effective and have fewer side effects than their racemic counterparts.
Used in Organic Synthesis:
[S,(-)]-α-Ethyl-α-methylbenzylamine is used as a chiral auxiliary in organic synthesis, where it aids in the creation of complex molecular structures with specific stereochemistry. This is particularly important for the development of new pharmaceuticals and other high-value chemicals.
Used in Asymmetric Catalysis:
As a ligand in asymmetric catalysis, [S,(-)]-α-Ethyl-α-methylbenzylamine plays a vital role in facilitating reactions with high enantioselectivity. This property is essential for producing optically active compounds, which are often required in the pharmaceutical and agrochemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 13088-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13088-92:
(7*1)+(6*3)+(5*0)+(4*8)+(3*8)+(2*9)+(1*2)=101
101 % 10 = 1
So 13088-92-1 is a valid CAS Registry Number.
13088-92-1Relevant academic research and scientific papers
COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS
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Page/Page column 45-49; 63, (2010/12/31)
The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.
Catalytic asymmetric synthesis using feedstocks: An enantioselective route to 2-arylpropionic acids and 1-arylethyl amines via hydrovinylation of vinyl arenes
Smith, Craig R.,Babu, T.V. Rajan
experimental part, p. 3066 - 3072 (2009/08/08)
A three-step procedure for the synthesis of 2-arylpropionic acids (profens) from vinyl arenes in nearly enantiomerically pure form has been developed. Excellent yields (>97%), regioselectivities (>99%), and enantioselectivities (>97% ee) for the desired branched products were obtained in the asymmetric hydrovinylation reactions of vinyl arenes, and the products from these reactions were transformed into 2-arylpropionic acids via oxidative degradation. Subsequent Curtius or Schmidt rearrangements of these acids provided highly valued 1-arylethyl amines, including a prototypical primary amine with an α-chiral tertiary N-alkyl group, in very good yields.
