91605-09-3 Usage
Molecular structure
The compound has a complex molecular structure that includes a diazabicyclooctane ring, a phenoxyacetyl group, a methylthio group, and a transconfiguration.
Diazabicyclooctane ring
This is a bicyclic ring system that contains two nitrogen atoms and is part of the compound's core structure.
Phenoxyacetyl group
This functional group is attached to the diazabicyclooctane ring and consists of a phenyl ring connected to an acetyl group.
Methylthio group
This functional group is also attached to the diazabicyclooctane ring and consists of a sulfur atom bonded to a methyl group.
Transconfiguration
The compound has a transconfiguration, which means that the phenoxyacetyl and methylthio groups are on opposite sides of the diazabicyclooctane ring.
Potential applications
Due to its unique structural features, the compound may have potential applications in various fields such as pharmaceuticals, agrochemicals, or material science.
Further research
Further research and analysis may be required to fully understand the properties and potential uses of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 91605-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,0 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91605-09:
(7*9)+(6*1)+(5*6)+(4*0)+(3*5)+(2*0)+(1*9)=123
123 % 10 = 3
So 91605-09-3 is a valid CAS Registry Number.
91605-09-3Relevant academic research and scientific papers
Stereospecific Synthesis of Some Novel cis-1-Aza Analogs of Cepham
Sharma, S. D.,Arora, S. K.,Mehra, Usha
, p. 895 - 901 (2007/10/02)
Annelation of N-acyl-2-thiomethyltetrahydropyrimidines (VII) with appropriate acid chlorides results in the formation of the corresponding β-methylthio-β-lactam (VIII) as single stereoisomer in each case.Treatment of these β-methylthio-β-lactams (VIII) with Ni in acetone yields stereospecifically the cis-1-azacepham analogs (IX).Application of a similar sequence of reactions on VIIf furnishes the novel 1-azacepham analog (XI) through a single step removal of the thiomethyl as well as the benzyloxycarbonyl groups from the intermediate β-lactam (X).Potassium carbethoxyacetonylglycinate (B) on treatment with the schiff base VIIa using POCl3/Et3N in CH2Cl2 gives the enamino-β-lactam (XII) which on exposure to HCl in ethanol yields the α-amino-β-lactam (XIV).Acylation of XIV with phenoxyacetyl chloride provides the α-amido-β-methylthio-β-lactam (XV).Raney-Ni desulphurisation of XII and XV affords ths cis-azacephams XIII and XVI respectively.
