52056-03-8 Usage
Chemical structure
A long hydrocarbon chain (octane) with a selenium atom attached at one end, and an octyl group (a type of alkyl group) attached at the other end.
Usage
Commonly used as a reagent in organic chemistry, particularly in the synthesis of organoselenium compounds.
Potential applications
Research and development of pharmaceuticals, due to the biological activities of organoselenium compounds.
Biological activities
Organoselenium compounds are known to exhibit antioxidant, anti-inflammatory, and anticancer properties.
Industrial and commercial uses
1-(octylselanyl)octane may have other industrial and commercial uses, but its specific applications and properties would depend on further research and development.
Further research
The specific applications and properties of 1-(octylselanyl)octane are not fully established and require additional research and development to determine its full potential.
Check Digit Verification of cas no
The CAS Registry Mumber 52056-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,5 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52056-03:
(7*5)+(6*2)+(5*0)+(4*5)+(3*6)+(2*0)+(1*3)=88
88 % 10 = 8
So 52056-03-8 is a valid CAS Registry Number.
52056-03-8Relevant academic research and scientific papers
Stereoselective synthesis of alkyl styryl selenides in one-pot: A straightforward approach by in situ dialkyl diselenide formation under transition metal-free conditions
Heredia, Adrián A.,Pe?é?ory, Alicia B.
, p. 105699 - 105706 (2015/12/26)
A simple procedure for the synthesis of alkyl styryl selenides was developed. This methodology involves the in situ generation of selenolate anions by a one-pot and three-step protocol where a nucleophilic substitution between KSeCN and alkyl halides affords the corresponding alkyl selenocyanate in the first step, giving dialkyl diselenide by a further K3PO4-assisted reaction. Subsequent reduction yields the alkyl selenolate anions which react with substituted (E,Z)-β-styryl halides to afford the corresponding vinyl selenides with retention of stereochemistry and from moderate to excellent yields. This procedure does not require a catalyst, proceeds under an air atmosphere and within a short reaction time, and is free from diselenide and malodorous and air-sensitive alkyl selenols as starting materials.
