4466-50-6 Usage
Uses
Used in Scientific Research:
N'-Isopropylacetohydrazide is used as a chemical intermediate for various chemical reactions, taking advantage of its unique structure and reactivity. This makes it a valuable compound in the field of scientific research.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, N'-Isopropylacetohydrazide is used as a key component in the synthesis of various pharmaceuticals. Its role in creating complex organic molecules contributes to the development of new drugs and medicinal compounds.
Used in Organic Chemistry:
N'-Isopropylacetohydrazide is employed as a reagent in organic chemistry, where it aids in the formation of new compounds and contributes to the advancement of chemical knowledge and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4466-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4466-50:
(6*4)+(5*4)+(4*6)+(3*6)+(2*5)+(1*0)=96
96 % 10 = 6
So 4466-50-6 is a valid CAS Registry Number.
4466-50-6Relevant academic research and scientific papers
BENZOXAZEPIN COMPOUNDS SELECTIVE FOR PI3K P110 DELTA AND METHODS OF USE
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Page/Page column 125, (2012/10/08)
Benzoxazepin Formula I compounds, including stereoisomers, geometric isomers, tautomers, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting the delta isoform of PI3K, and for treating disorders mediated by lipid kinases such as inflammation, immunological disorders, and cancer. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
1-Acyl-2-alkylhydrazines by the Reduction of Acylhydrazones
Pei-Lin-Wu,Peng, Shao-Yu,Magrath, Joe
, p. 435 - 438 (2007/10/02)
1-Acyl-2-alkylhydrazines were easily prepared by the reduction of acylhydrazones with triethylsilane in the presence of trifluoroacetic acid.
