61395-07-1 Usage
Appearance
Yellow to brown colored solid The substance has a yellow to brown color and is a solid in its physical form.
Solubility
Soluble in organic solvents such as ethanol and acetone 2-(1-oxidopyridin-2-yl)-1-phenylethanone can dissolve in certain organic solvents, specifically ethanol and acetone.
Uses
Building block in organic synthesis and pharmaceutical research 2-(1-oxidopyridin-2-yl)-1-phenylethanone is commonly used as a starting material in the synthesis of other organic compounds and as a building block in the development of new drugs.
Potential applications
Development of new drugs and synthesis of biologically active compounds 2-(1-oxidopyridin-2-yl)-1-phenylethanone has been studied for its potential use in creating new medications and other biologically active substances.
Antioxidant and antibacterial properties
Potential candidate for further investigation in medicine and healthcare 2-(1-oxidopyridin-2-yl)-1-phenylethanone has been reported to possess properties that may make it useful in the prevention of oxidative damage and the inhibition of bacterial growth, making it a promising candidate for further research in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 61395-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61395-07:
(7*6)+(6*1)+(5*3)+(4*9)+(3*5)+(2*0)+(1*7)=121
121 % 10 = 1
So 61395-07-1 is a valid CAS Registry Number.
61395-07-1Relevant academic research and scientific papers
2-heterocyclicethylamine derivatives and their use as pharmaceuticals
-
, (2008/06/13)
Compounds of formula (I), wherein A represents CH=CH; Q represents pyrazine having substituents R6 and R7 ; R1 represents H or C1-6 alkyl; R2 represents H, C1-6 alkyl, C3-6 alken
1-Substituted-2-(2-pyridinyl)ethanone N-oxides
-
, (2008/06/13)
1-Substituted-2-(2-pyridinyl)ethanone N-oxides having the formula I or II: STR1 wherein R1 is hydrogen or lower alkyl; R2 and R3 are each hydrogen, halogen, hydroxy, lower alkyl, lower alkoxy, or benzyloxy; R4 i
