34208-81-6 Usage
Uses
Used in Pharmaceutical Industry:
[(1β,4β,7-anti)-Bicyclo[2.2.1]hept-2-en-7-yl]trimethylstannane is used as a potential therapeutic agent for its anti-inflammatory and analgesic properties, which can be beneficial in the treatment of various conditions characterized by inflammation and pain.
Used in Organic Synthesis:
In the field of organic chemistry, [(1β,4β,7-anti)-Bicyclo[2.2.1]hept-2-en-7-yl]trimethylstannane is used as a reagent, particularly for the formation of carbon-carbon bonds. Its unique structure and properties make it a valuable tool for researchers and chemical engineers in the development of new synthetic pathways and the creation of novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 34208-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,0 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34208-81:
(7*3)+(6*4)+(5*2)+(4*0)+(3*8)+(2*8)+(1*1)=96
96 % 10 = 6
So 34208-81-6 is a valid CAS Registry Number.
34208-81-6Relevant academic research and scientific papers
Nucleophilic substitution of bromonorbornenes and derivatives by electron transfer reactions
Crespo Andrada, Karina F.,Peisino, Lucas E.,Gueney, Murat,Dastan, Arif,Pierini, Adriana B.
, p. 955 - 965 (2013/02/26)
The photoinitiated substitution reactions of anti-7-bromobenzonorbornadiene (5), its syn isomer 6, exo-anti-13-bromobenzocyclobutanorbornene (7), syn-7-bromonorbornene (8) and bromonorbornane (9) with Me3Sn - and Ph2P- anions, in liquid ammonia, are here informed to occur with good yields of substitution. The stereochemical outcome is discussed in terms of calculations with the B3LYP functional and the 6-31+G* basis set; the solvent being included as a continuum through the PCM model. The experimental relative chemical reactivity of pairs of substrates toward a given anion is also presented.
