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(1R,2R,7S,8S)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.0^2,7^]undeca-3,9-dien-6-one is a complex organic compound characterized by its unique molecular structure. It features a tricyclic ring system with a 5-membered oxa (oxygen-containing) ring and a 3-membered aza (nitrogen-containing) ring, fused to a 6-membered carbon ring. The compound has a 4-chlorophenyl group attached to the tricyclic core, which contributes to its chemical properties. The numbering of the carbon atoms in the molecule is such that the 4-position is occupied by the chlorophenyl group, and the 6-position is the site of the carbonyl group, indicating a ketone functionality. The stereochemistry is specified by the R, S configuration at the 1, 2, 7, and 8 positions, which defines the three-dimensional arrangement of the atoms in the molecule. (1R,2R,7S,8S)-4-(4-Chloro-phenyl)-5-oxa-3-aza-tricyclo[6.2.1.02,7]undeca-3,9-dien-6-one is likely to be of interest in the field of organic chemistry, potentially for its reactivity or as a building block in the synthesis of more complex molecules.

91813-52-4

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91813-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91813-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,1 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91813-52:
(7*9)+(6*1)+(5*8)+(4*1)+(3*3)+(2*5)+(1*2)=134
134 % 10 = 4
So 91813-52-4 is a valid CAS Registry Number.

91813-52-4Relevant academic research and scientific papers

STEREOCHEMICAL STUDIES -- 79 SYNTHESIS AND KINETIC STUDY ON THE RETRODIENE DECOMPOSITION OF NORBORNENE-CONDENSED 1,3-OXAZIN-4-ONES

Stajer, Geza,Mod, Laszlo,Szabo, Angela E.,Fueloep, Ferenc,Bernath, Gabor,Sohar, Pal

, p. 2385 - 2393 (2007/10/02)

The cis-exo-amino acid 3 with norbornene skeleton was converted into 2-aryl-cis-exo-1,3-oxazin-4-ones 5a-d.These compounds, similarly to the diendo isomers 1a-d studied by us earlier, undergo retrodiene decomposition under mild conditions to give 2-aryl-6

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