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(3R,6S,7S)-6-Hydroxy-5,9-dioxo-3-phenyl-4-aza-tricyclo[4.3.0.0^3,7^]nonane-7-carboxylic acid ethyl ester is a complex organic compound with a molecular formula of C18H21NO5. It features a tricyclic structure with a nitrogen atom in the 4-position, a phenyl group at the 3-position, and a carboxylic acid group at the 7-position. The compound is characterized by its 3R, 6S, and 7S stereochemistry, indicating the specific spatial arrangement of its atoms. The hydroxyl group at the 6-position and the two carbonyl groups at the 5 and 9 positions contribute to its reactivity and functional properties. The ethyl ester group at the carboxylic acid endows the molecule with additional solubility and reactivity characteristics. (3R,6S,7S)-6-Hydroxy-5,9-dioxo-3-phenyl-4-aza-tricyclo[4.3.0.03,7]nonane-7-carboxylic acid ethyl ester is likely to be found in pharmaceutical or chemical research settings, where its unique structure could be exploited for specific applications, such as in the development of new drugs or as an intermediate in organic synthesis.

80053-95-8

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80053-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80053-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80053-95:
(7*8)+(6*0)+(5*0)+(4*5)+(3*3)+(2*9)+(1*5)=108
108 % 10 = 8
So 80053-95-8 is a valid CAS Registry Number.

80053-95-8Relevant academic research and scientific papers

Dioxopyrroline. L. Skeletal rearrangements of 7-vinyl-7-trimethylsilyloxy-5-ethoxycarbonyl-1-phenyl-2-azabicyclo[3.2. 0]heptane-3,5-diones under thermal, basic, and acidic conditions

Sano,Toda,Tsuda

, p. 36 - 42 (2007/10/02)

The oxyvinylcyclobutanes (2), photoadducts of the dioxopyrrolines (1) to trimethylsilyloxybutadienes, undergo two different types of skeletal rearrangements depending on the reaction conditions. Thermolysis of 2 caused expansion of the cyclobutane ring by

FACILE OXY-VINYL SHIFT PROMOTED BY TETRABUTYLAMMONIUM FLUORIDE: A HYDROINDOLE SYNTHESIS

Sano, Takehiro,Toda, Jun,Tsuda, Yoshisuke

, p. 2960 - 2962 (2007/10/02)

The oxy-vinyl alkoxides generated from trimethylsilyloxy-vinyl (or methoxyvinyl)-cyclobutanes by tetra-n-butylammonium fluoride undergo a facile shift to produce a two-carbon unit ring expansion compound under extremely mild conditions.Thus, 7-trimet

2-AZABICYCLOHEPTANE-3,4-DIONES (6) A NOVEL METHOD OF REGIO-CONTROLLED SYNTHESIS OF FUNCTIONALIZED HYDROINDOLES AND ERYTHRINAN DERIVATIVES

Sano, Takehiro,Toda, Jun,Horiguchi, Yoshie,Imafuku, Kazue,Tsuda, Yoshisuke

, p. 1463 - 1468 (2007/10/02)

A regio-controlled synthesis of functionalized hydroindoles from a Δ2-pyrrolinedione and its application to the synthesis of erythrinan skeleton were described.The method is to construct with photocycloaddition of a trimethylsilyloxybutad

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