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(1S,4S,5S)-4-[2-(2-Nitro-phenylselanyl)-ethyl]-2,8-dioxa-bicyclo[3.3.1]nonane is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by its specific stereochemistry, with the 1, 4, and 5 positions being in the S configuration. The compound features a bicyclo[3.3.1]nonane ring system, which is a type of bridged bicycle, and a 2-nitro-phenylselanyl group attached to an ethyl chain. This group contains a selenium atom bonded to a 2-nitrophenyl group, which is an aromatic ring with a nitro group at the 2-position. The presence of the nitro group and the selenium atom contribute to the compound's reactivity and potential applications in various chemical and pharmaceutical contexts.

85184-46-9

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85184-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85184-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85184-46:
(7*8)+(6*5)+(5*1)+(4*8)+(3*4)+(2*4)+(1*6)=149
149 % 10 = 9
So 85184-46-9 is a valid CAS Registry Number.

85184-46-9Downstream Products

85184-46-9Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF (+/-)-SEMBURIN AND (+/-)-ISOSEMBURIN USING A COMMON BICYCLIC PRECURSOR

Takano, Seiichi,Morimoto, Masamichi,Masuda, Ken'ichi,Ogasawara, Kunio

, p. 4238 - 4241 (2007/10/02)

Using the common bicyclic compound 1-oxabicyclooctan-2-one (1), two isomeric monoterpenes, semburin (6) and isosemburin (7) isolated from Swertia japonica Makino, have been synthesized stereoselectively in racemic forms.Keywords - 2,8-dioxabicyclononane; semburin; isosemburin; stereoselective synthesis; kinetic protonation; α-diketone monothioketal

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