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trans-(3R,4S)-1(R)-(α-methylbenzyl)-3-(2,2,5,5-tetramethyl-1-aza-2,5-disilacyclopentyl)-4--2-azetidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129086-49-3

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129086-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129086-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,8 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129086-49:
(8*1)+(7*2)+(6*9)+(5*0)+(4*8)+(3*6)+(2*4)+(1*9)=143
143 % 10 = 3
So 129086-49-3 is a valid CAS Registry Number.

129086-49-3Downstream Products

129086-49-3Relevant academic research and scientific papers

Enantioselective Synthesis of a Chiral Intermediate for Aztreonam and Related Monobactam Antibiotics

Steen, Fred H. van der,Kleijn, Henk,Spek, Anthony L.,Koten, Gerard van

, p. 503 - 504 (1990)

The enantioselective synthesis of trans-(3R,4S)-1-(R)-α-methylbenzyl-3-(2,2,5,5-tetramethyl-1-aza-2,5-disilacyclopentyl)-4-N-(R)-α-methylbenzyliminoazetidin-2-one has been accomplished by reaction of the chlorozinc enolate of an N,N-diprotected glycine ethyl ester with a chiral α-diimine.

Enantioselective Synthesis of 3-Amino-2-azetidinones via the Ester Enolate-Imine Condensation

Steen, Fred H. van der,Kleijn, Henk,Britovsek, George J. P.,Jastrzebski, Johann T. B. H.,Koten, Gerard van

, p. 3906 - 3916 (2007/10/02)

Three approaches to the enantioselective synthesis of 3-amino-4-substituted-2-azetidinones by condensation of α-amino ester enolates with imines are described: (i) application of chiral ester derivatives of N,N-diethylglycine; (ii) application of chiral N

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