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Specific stereoisomer of azetidinone with an ethyl group, methylene group, and phenylmethyl group

293307-40-1

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293307-40-1 Usage

Chemical compound

2-Azetidinone, 4-ethyl-3-methylene-1-(phenylmethyl)-,(4R)-(9CI)

Stereochemistry

4R absolute configuration

Usage

Building block in pharmaceutical and organic compound synthesis

Reactivity

Versatile functional groups
Potential biological activities

Applications

Medicinal and pharmaceutical applications

Check Digit Verification of cas no

The CAS Registry Mumber 293307-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,0 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 293307-40:
(8*2)+(7*9)+(6*3)+(5*3)+(4*0)+(3*7)+(2*4)+(1*0)=141
141 % 10 = 1
So 293307-40-1 is a valid CAS Registry Number.

293307-40-1Downstream Products

293307-40-1Relevant articles and documents

Synthesis of Optically Active α-Methylene β-Lactams through Lipase-Catalyzed Kinetic Resolution

Adam, Waldemar,Groer, Peter,Humpf, Hans-Ulrich,Saha-Moeller, Chantu R.

, p. 4919 - 4922 (2007/10/03)

A convenient method for the preparation of the hitherto unknown chiral α-methylene β-lactam derivatives 5a,b is reported. The optically active α-methylene β-lactams 5a-c, and their corresponding amino acids 6a-c have been readily made available through li

Synthesis of optically active α-methylene β-lactams through lipase-catalyzed kinetic resolution

Adam, Waldemar,Groer, Peter,Humpf, Hans-Ulrich,Saha-Moeller, Chantu R.

, p. 4919 - 4922 (2007/10/03)

A convenient method for the preparation of the hitherto unknown chiral α-methylene β-lactam derivatives 5a,b is reported. The optically active α-methylene β-lactams 5a-c, and their corresponding amino acids 6a-c have been readily made available through lipase-catalyzed kinetic resolution in high enantiomeric purity (up to 99% ee). The N-substituted β-lactam derivatives 4a,b and 10 are not accepted by the lipases and were prepared in optically active form by chemical transformation.

Synthesis of 3-Methyleneazetidin-2-one Derivatives from α-Keto-amides

Adlington, Robert M.,Barrett, Anthony G.M.,Quayle, Peter,Walker, Andrew,Betts, Michael J.

, p. 605 - 612 (2007/10/02)

Several α-methyleneazetidin-2-one derivatives (CH2=CCONR1CHR2, R1 = cyclohexyl, PhCH2; R2 = H, Me, Et, Prn, etc.) were prepared from the 2-(2,4,6-tri-isopropylbenzenesulphonylhydrazones) of primary α-

Novel Syntheses of 3-Methylene-azetidin-2-one Derivatives and Related Systems

Adlington, Robert M.,Barrett, Anthony G. M.,Quayle, Peter,Walker, Andrew,Betts, Michael J.

, p. 404 - 405 (2007/10/02)

Syntheses of the title compounds via 1-lithio-oxy-1-lithio-amino-allene derivatives or lithium phenylethynolate are described.

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