1260785-45-2 Usage
Description
1-(4-hydroxy-3-methoxy-2-nitrophenyl)ethanone is a chemical compound characterized by a benzene ring with a hydroxyl group, a methoxy group, and a nitro group attached to it, along with an ethanone group. 1-(4-hydroxy-3-methoxy-2-nitrophenyl)ethanone is known for its potential medicinal properties due to the antioxidant and anti-inflammatory activities of the hydroxyl and methoxy groups, while the nitro group can influence biological systems in various ways. However, caution is advised due to the possible toxicity associated with the nitro group.
Uses
Used in Pharmaceutical Industry:
1-(4-hydroxy-3-methoxy-2-nitrophenyl)ethanone is used as an intermediate in the synthesis of pharmaceuticals for its potential medicinal properties. The hydroxyl and methoxy groups in the compound contribute to antioxidant and anti-inflammatory activities, making it a valuable component in the development of new drugs.
Used in Organic Synthesis:
In the chemical industry, 1-(4-hydroxy-3-methoxy-2-nitrophenyl)ethanone serves as an important intermediate in organic synthesis. Its unique structure allows for further chemical reactions and modifications, leading to the creation of a variety of other compounds with different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1260785-45-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,7,8 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1260785-45:
(9*1)+(8*2)+(7*6)+(6*0)+(5*7)+(4*8)+(3*5)+(2*4)+(1*5)=162
162 % 10 = 2
So 1260785-45-2 is a valid CAS Registry Number.
1260785-45-2Relevant articles and documents
Synthesis and biological evaluation of a novel series of "ortho-nitrated" inhibitors of catechol-O-methyltransferase
Learmonth, David A.,Bonifácio, Maria Jo?o,Soares-Da-Silva, Patricio
, p. 8070 - 8078 (2007/10/03)
Novel regioisomeric "ortho-nitrated" catechols related to the catechol-O-methyltransferase (COMT) inhibitors BIA 3-202 3 and BIA 3-335 4 were synthesized and biologically evaluated. Changing the position of the nitro group from the "classical" meta- to th
