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The chemical compound "(1S)-6-hydroxy-9-(1-hydroxy-1-methyl-ethyl)-5-methylene-8,10-dioxo-2-oxa-7,9-diaza-bicyclo[4.2.2]decane-1-carbaldehyde 1,9-cyclohemiacetal" is a complex organic molecule with a unique structure. It features a bicyclo[4.2.2]decane ring system, which is a type of fused ring structure consisting of two six-membered rings. The molecule contains a carbaldehyde group, indicating the presence of a carbonyl group at the end of a carbon chain. Additionally, it has a 1,9-cyclohemiacetal functional group, which is a type of acetal formed by the reaction of an aldehyde with an alcohol, protecting the aldehyde group from further reactions. The compound also includes a 5-methylene group, which is a carbon-carbon double bond with one hydrogen atom attached to the carbon. The presence of hydroxyl groups and the 2-oxa bridge further contribute to the molecule's complexity and reactivity. (1S)-6-hydroxy-9-(1-hydroxy-1-methyl-ethyl)-5-methylene-8,10-dioxo-2-oxa-7,9-diaza-bicyclo[4.2.2]decane-1-carbaldehyde 1,9-cyclohemiacetal is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex molecules due to its intricate structure and functional groups.

71994-04-2

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71994-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71994-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71994-04:
(7*7)+(6*1)+(5*9)+(4*9)+(3*4)+(2*0)+(1*4)=152
152 % 10 = 2
So 71994-04-2 is a valid CAS Registry Number.

71994-04-2Downstream Products

71994-04-2Relevant academic research and scientific papers

Semisynthetic bicyclomycin derivatives: Preparation and antibacterial evaluation

Muller,Zak,Kump,Tosch,Wacker

, p. 689 - 705 (1979)

A number of semisynthetic bicyclomycin derivatives have been prepared by modifications at various sites of the molecule. The preparation, characterization and antimicrobial evaluation of the new compounds is described. In contrast to bicyclomycin itself,

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