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The chemical compound "(6R)-3-acetoxymethyl-8-oxo-7t-(2-phenyl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2ξ-carboxylic acid" is a complex organic molecule with a unique structure. It features a bicyclic ring system with a thiazole and an azabicyclo[4.2.0]octane core, which is a type of heterocyclic compound. The molecule contains an acetoxymethyl group at the 3-position, an oxo group at the 8-position, and a phenyl-acetylamino group at the 7-position, which is part of a trans (t) configuration. The compound also has a carboxylic acid group at the 2ξ-position, indicating its acidic nature. This chemical is characterized by its chirality, with the 6R configuration indicating the specific arrangement of atoms in the molecule. The presence of multiple functional groups, such as the acetoxymethyl, oxo, and carboxylic acid groups, suggests that (6R)-3-acetoxymethyl-8-oxo-7t-(2-phenyl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2ξ-carboxylic acid may have diverse chemical reactivity and potential applications in various fields, including pharmaceuticals and materials science.

805-64-1

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805-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 805-64-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 805-64:
(5*8)+(4*0)+(3*5)+(2*6)+(1*4)=71
71 % 10 = 1
So 805-64-1 is a valid CAS Registry Number.

805-64-1Upstream product

805-64-1Relevant academic research and scientific papers

Synthesis and antibacterial activity of dual-action agents of a β-lactam antibiotic with cytotoxic agent mitozolomide or temozolomide

Wang, Yongfeng,Lambert, Peter,Zhao, Linxiang,Wang, Danni

, p. 323 - 332 (2007/10/03)

Dual-action agents 5a-f and 12a-f, a β-lactam antibiotic combined with a cytotoxic agent, mitozolomide (Meto) or temozolomide (Temo), were synthesised. The antibacterial activity (MICs) of the dual-action agents has been determined against a panel of bacteria including several β-lactamase producing strains. The tests showed 5a-f active against the non-β-lactamase producing methicillin sensitive Staphylococcus aureus (MSSA) strains, however, little synergistic effect between the β-lactam and the cytotoxic agent was observed. 12a-f demonstrated some synergistic effect against bacteria. 12a, in particular, is active against ampicillin resistant (β-lactamase-producing) strains of Serratia marcescens.

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