111922-90-8 Usage
Chemical structure
A unique combination of a ketone functional group, a morpholine ring, and a nitrophenyl group.
Usage
Commonly used in organic synthesis as a reagent for the formation of various organic compounds.
Industries
A valuable synthetic intermediate in the pharmaceutical and agrochemical industries.
Biological activities
Known for its potent biological activities, particularly its anti-inflammatory and anti-cancer properties.
Research and development
Presence in various fields and its biological activities make this chemical a compound of interest for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 111922-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 111922-90:
(8*1)+(7*1)+(6*1)+(5*9)+(4*2)+(3*2)+(2*9)+(1*0)=98
98 % 10 = 8
So 111922-90-8 is a valid CAS Registry Number.
111922-90-8Relevant articles and documents
Enamines: Part IV - Synthesis of Nitro Substituted Alkyl Phenyl Ketones
Kulkarni, Sheshgiri N.,Bhamare, N. K.,Kamath, H. V.
, p. 168 - 170 (2007/10/02)
Nitro substituted alkyl phenyl ketones (V) have been synthesised by reacting nitro substituted benzoyl chlorides (II) with morpholine enamines (I) of aliphatic aldehydes.The resulting acylated enamines (III) on hydrolysis afford the desired V.However, 2-n
