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tert-Butyl (4S)-3-<(2S)-2-(N-benzylamino)butyryl>-1-methyl-2-oxoimidazolidine-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

166903-71-5

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166903-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166903-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,9,0 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 166903-71:
(8*1)+(7*6)+(6*6)+(5*9)+(4*0)+(3*3)+(2*7)+(1*1)=155
155 % 10 = 5
So 166903-71-5 is a valid CAS Registry Number.

166903-71-5Downstream Products

166903-71-5Relevant academic research and scientific papers

Dynamic Kinetic Resolution of Racemic α-halo Acids via a Chiral Imidazolidinone Auxiliary

O'Meara, Jeff A.,Jung, Manfred,Durst, Tony

, p. 2559 - 2562 (1995)

A dynamic kinetic resolution is utilized to realize highly diastereoselective nucleophilic displacement of bromine in tert-butyl (4S)-1-methyl-3-(2-bromoacyl)-2-oxoimidazolidine-4-carboxylates (6a-f) by benzylamine enroute to tert-butyl (4S)-1-methyl-3-(2

Stereospecific Amination by Dynamic Kinetic Resolution Utilizing 2-Oxoimidazolidine-4-carboxylate as a Novel Chiral Auxiliary

Kubota, Hitoshi,Kubo, Akira,Takahashi, Masami,Shimizu, Ryo,Da-te, Tadamasa,et al.

, p. 6776 - 6784 (2007/10/03)

A novel type of stereospecific amination by dynamic kinetic resolution using (4S)-2-oxoimidazolidine-4-carboxylate (1) as a chiral auxiliary was developed. A reaction of a diastereomeric mixture of (4S)-3--2-oxoimidazolidine-4-carboxylates 4 with an amine in the presence of a base in HMPA predominantly afforded (4S)-3--2-oxoimidazolidine-4-carboxylates (S,R)-7 in good yields.The reaction proceeded by stereospecific SN2 type amination incorporated with rapid interconversion between the substrates (S,S)-4 and (S,R)-4.Mechanistic study suggested that the unique stereoselectivity was induced through the interaction between an amine and the ester group of (S,S)-4 in the transition state.The chiral auxiliary was easily removed with alkoxide anion to afford the α-amino acid synthon in good yields.

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