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(1S,4R,5S,6R)-5-(2,4-Dichloro-phenyl)-6-nitro-bicyclo[2.2.1]hept-2-ene is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the 1, 4, 5, and 6 positions being in the S or R configuration. The compound features a bicyclo[2.2.1]hept-2-ene ring system, which is a type of bridged bicyclic compound with seven carbon atoms. One of the phenyl rings in the molecule is substituted with two chlorine atoms at the 2 and 4 positions, and the other phenyl ring is substituted with a nitro group at the 6 position. (1S,4R,5S,6R)-5-(2,4-Dichloro-phenyl)-6-nitro-bicyclo[2.2.1]hept-2-ene is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its specific functional groups and stereochemistry.

92023-55-7

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92023-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92023-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92023-55:
(7*9)+(6*2)+(5*0)+(4*2)+(3*3)+(2*5)+(1*5)=107
107 % 10 = 7
So 92023-55-7 is a valid CAS Registry Number.

92023-55-7Relevant academic research and scientific papers

Synthese d'aryl nitronorbornenes par cycloaddition de Diels-Alder entre les aryl-nitroethylenes et le cyclopentadiene. Justification de la stereochimie et de la reactivite relative observees par la methode CNDO/II. Obtention d'aryl aminonorbornenes

Bourguignon, Jean,Le Nard, Gilles,Queguiner, Guy

, p. 2354 - 2361 (2007/10/02)

Syntheses of numerous 2-aryl nitroethylenes (nitrostyrenes) have been optimized.The nitrostyrenes have been reacted with cyclopentadiene in Diels-Alder cycloadditions and the 3-aryl 2-nitronorbornenes obtained have been reduced into 3-aryl 2-aminonorbornenes.These compounds are potentially dopaminergic molecules.The stereochemistry of the adducts obtained in the Diels-Alder reaction has been determined by 1H nmr.The stereochemistry and the relative reactivity of the nitrostyrenes versus cyclopentadiene have been confirmed by theoretical calculations based on the CNDO/II method.

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