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(1S,4R,5S,6S)-5-Chloro-2,2-dimethoxy-6-phenylselanyl-bicyclo[2.2.1]heptane is a complex organic compound with a unique molecular structure. It is characterized by a bicyclo[2.2.1]heptane ring system, which consists of two carbon rings fused together in a specific arrangement. The compound features a chloro group at the 5-position, two methoxy groups at the 2-position, and a phenylselanyl group at the 6-position. The phenylselanyl group is a phenyl group bonded to a selenium atom, which adds a unique element to the compound's properties. The stereochemistry of the compound is defined by the (1S,4R,5S,6S) configuration, indicating the specific arrangement of atoms in three-dimensional space. (1S,4R,5S,6S)-5-Chloro-2,2-dimethoxy-6-phenylselanyl-bicyclo[2.2.1]heptane is of interest in organic chemistry and may have potential applications in various fields, such as pharmaceuticals or materials science, due to its unique structure and properties.

83205-39-4

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83205-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83205-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,0 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83205-39:
(7*8)+(6*3)+(5*2)+(4*0)+(3*5)+(2*3)+(1*9)=114
114 % 10 = 4
So 83205-39-4 is a valid CAS Registry Number.

83205-39-4Downstream Products

83205-39-4Relevant academic research and scientific papers

REGIOSELECTIVE ADDITIONS OF ELECTROPHILES TO OLEFINS REMOTELY PERTURBED. THE CARBONYL GROUP AS A HOMOCONJUGATED ELECTRON DONATING SUBSTITUENT.

Carrupt, Pierre-Alain,Vogel, Pierre

, p. 2563 - 2566 (2007/10/02)

Electrophiles attack preferentially at the C(5) position of 2-norborn-5-enone and 2-bicyclooct-5-enone whereas the C(6) position is preferred for 2-chloronorborn-5-ene-2-carbonitriles and 2-chlorobicyclooct-5-ene-2-carbonitriles.

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