880634-13-9 Usage
Chemical structure
Contains a tetrazole ring, a sulfonyl group, and a phenyl group, with a bromomethyl group attached to the sulfur atom in the sulfonyl group.
Common uses
Used as a reagent in organic synthesis and as a precursor for the synthesis of pharmaceuticals, agrochemicals, and materials.
Reactivity
Known for its reactivity and is often utilized in the formation of carbon-nitrogen bonds in various organic reactions.
Unique structure and properties
Valuable building block for the preparation of diverse functionalized compounds with potential applications in the fields of medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 880634-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,0,6,3 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 880634-13:
(8*8)+(7*8)+(6*0)+(5*6)+(4*3)+(3*4)+(2*1)+(1*3)=179
179 % 10 = 9
So 880634-13-9 is a valid CAS Registry Number.
880634-13-9Relevant academic research and scientific papers
Stereoselective synthesis of Z alkenyl halides via Julia olefination
Lebrun, Marie-Eve,Le Marquand, Paul,Berthelette, Carl
, p. 2009 - 2013 (2007/10/03)
Julia olefination between α-halomethyl sulfones and a variety of aldehydes afforded alkenyl halides in good to excellent yields with high E/Z stereoselectivities. Sulfones were readily prepared in two or three steps from commercially available reagents in good yields. Optimization revealed that the nature of the solvent, the base, and the additive were crucial to obtain the desired alkenyl halides.
