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(1S,4R,5R,6R)-6-Chloro-2,2-dimethoxy-5-phenylselanyl-bicyclo[2.2.1]heptane is a complex organic compound characterized by its unique molecular structure. It features a bicyclo[2.2.1]heptane ring system, which consists of two carbon rings fused together in a specific arrangement. The compound is further defined by its stereochemistry, with four chiral centers at positions 1, 4, 5, and 6, all having the R configuration except for position 1, which has the S configuration. It contains a chloro group at the 6-position, two methoxy groups, and a phenylselanyl group at the 5-position, which introduces a phenyl ring attached to a selenium atom. (1S,4R,5R,6R)-6-Chloro-2,2-dimethoxy-5-phenylselanyl-bicyclo[2.2.1]heptane is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structural features and potential reactivity.

83205-35-0

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83205-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83205-35-0 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 83205-35:
(7*8)+(6*3)+(5*2)+(4*0)+(3*5)+(2*3)+(1*5)=110
110 % 10 = 0
So 83205-35-0 is a valid CAS Registry Number.

83205-35-0Downstream Products

83205-35-0Relevant 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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