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cis-1-benzyl-4-[(3aαH,8bαH)-tetrahydro-2,2,7,7-tetrahydro-2,2,7,7-tetramethyl-5H-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran-5-yl]-3-methoxy-azetidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161972-97-0

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161972-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161972-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,7 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161972-97:
(8*1)+(7*6)+(6*1)+(5*9)+(4*7)+(3*2)+(2*9)+(1*7)=160
160 % 10 = 0
So 161972-97-0 is a valid CAS Registry Number.

161972-97-0Relevant academic research and scientific papers

Polyhydroxy amino acid derivatives via β-lactams using enantiospecific approaches and microwave techniques

Bose, Ajay K.,Banik, Bimal K.,Mathur, Chandra,Wagle, Dilip R.,Manhas, Maghar S.

, p. 5603 - 5619 (2007/10/03)

Enantiospecific synthesis has been developed for α-hydroxy β-lactams of predictable absolute configuration starting with readily available carbohydrates. Stereospecific approaches and microwave assisted chemical reactions have been utilized for the prepar

CHIRAL β-LACTAMS AS SYNTHONS. STEREOSPECIFIC SYNTHESIS OF A 6-EPI-LINCOSAMINE DERIVATIVE

Bose, Ajay K.,Mathur, Chandra,Wagle, Dilip R.,Naqvi, Raza,Manhas, Maghar S.,Urbanczyk-Lipkowska, Zofia

, p. 491 - 496 (2007/10/02)

A derivative of 6-epi-lincosamine has been prepared by a sequence of stereospecific steps from an optically active, cis-α-hydroxy-β-lactam.This β-lactam was obtained by an enantiospecific cycloaddition reaction between methoxyacetyl chloride, triethylamin

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