2417-90-5 Usage
Description
3-BROMOPROPIONITRILE, also known as 3-bromo-1-cyanopropene, is a clear colorless to light yellow liquid with chemical properties that make it a versatile compound in various applications. It is characterized by its bromine atom and nitrile group, which contribute to its reactivity and utility in chemical reactions.
Uses
Used in Polymer Synthesis:
3-BROMOPROPIONITRILE is used as an initiator for [atom transfer radical polymerization] for [the controlled growth of polymer chains]. This application is particularly relevant in the production of polymers with specific properties and structures, such as acrylonitrile polymers.
Used in Pharmaceutical Industry:
3-BROMOPROPIONITRILE is used as a coupling agent for [reactions involving aromatic and heteroaromatic phenols] with [alkyl, acyl, or benzoyl halides] in acetonitrile with cesium fluoride-Celite. This application is crucial in the synthesis of various pharmaceutical compounds, as it facilitates the formation of new carbon-carbon bonds and the creation of complex molecular structures.
Used in Chemical Synthesis:
3-BROMOPROPIONITRILE is used as a reagent for [various chemical reactions] due to [its reactivity and the presence of the bromine atom and nitrile group]. This application is important in the synthesis of a wide range of chemicals, including those used in the production of dyes, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 2417-90-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2417-90:
(6*2)+(5*4)+(4*1)+(3*7)+(2*9)+(1*0)=75
75 % 10 = 5
So 2417-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H4BrN/c4-2-1-3-5/h1-2H2
2417-90-5Relevant articles and documents
Fujiyama
, p. 3317 (1971)
One-pot synthesis of aryl sulfones from alcohols
Murakami, Teiichi,Furusawa, Kiyotaka
, p. 479 - 482 (2007/10/03)
A one-pot synthesis of aryl sulfones from primary alcohols is described. Alcohols were treated with N-bromosuccinimide and triphenylphosphine, followed by addition of sodium arenesulfinate with a catalytic amount of tetrabutylammonium iodide to afford the aryl sulfones in good to high yields.
