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1-(1-carboxy-2-methylprop-2-enyl)-3-phenylacetamido-4-(1,5,5-trimethylhydantoin-3-yl)-thio-azetidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54172-83-7

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54172-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54172-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,7 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54172-83:
(7*5)+(6*4)+(5*1)+(4*7)+(3*2)+(2*8)+(1*3)=117
117 % 10 = 7
So 54172-83-7 is a valid CAS Registry Number.

54172-83-7Downstream Products

54172-83-7Relevant academic research and scientific papers

Acetidine derivatives

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, (2008/06/13)

A new azetidine derivative of the formula: EQU1 wherein R1 represents a penicillin- or cephalosporin-amido group, R2 represents one of the groups of the following formulae: EQU2 wherein R4, R5 and R6 are the same or different and each represents a hydrogen atom or a lower alkyl or alkenyl group, n represents 2 or 3 and - in case formula IIB represents a phenyl group - this group may carry one to four further substituents selected from the group consisting of halogen atoms and lower alkyl, lower alkenyl and phenyl groups, R3 represents an amino group of the formula EQU3 wherein R7 represents a hydrogen atom or a lower alkyl group and R8 represents a lower alkyl group, or R3 represents a N,N'-disubstituted hydrazino group wherein the substituents are lower alkyl groups, e.g. the N,N'-diisopropylhydrazino group, or R3 represents the group --OR9, wherein R9 represents a hydrogen atom, a lower alkyl group, which group may be substituted by 1 to 3 halogen atoms or by 1 or 2 phenyl groups, werein the phenyl groups may be substituted by a methoxy or a nitro group, or R9 represents a phenacyl group or a salt-forming cation, And corresponding azetidine derivatives of formula I wherein the double bond in the propenyl side chain has been shifted from the 2- to the 1-position, which are versatile intermediates in the process of preparing cephalosporanic and penicillanic derivative.

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