941-95-7 Usage
Heterocyclic compound
Phthalazine ring 2-(hydroxymethyl)phthalazin-1(2H)-one contains a phthalazine ring, which is a heterocyclic aromatic ring consisting of a six-membered ring with alternating single and double bonds, and two nitrogen atoms in the ring.
Hydroxymethyl group
Attached to a carbon atom A hydroxymethyl group (-CH2OH) is attached to one of the carbon atoms in the phthalazine ring, making the compound more reactive and functional.
Biological activities
Anti-inflammatory and anti-tumor properties 2-(hydroxymethyl)phthalazin-1(2H)-one has potential therapeutic applications due to its ability to reduce inflammation and inhibit tumor growth.
Building block in organic synthesis
Production of other chemical compounds 2-(hydroxymethyl)phthalazin-1(2H)-one can be used as a starting material or intermediate in the synthesis of other chemical compounds, making it a valuable asset in the field of organic chemistry.
Versatility
Unique structure and functional groups The combination of the phthalazine ring, hydroxymethyl group, and other functional groups in 2-(hydroxymethyl)phthalazin-1(2H)-one makes it a potentially valuable compound for various applications in chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 941-95-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 941-95:
(5*9)+(4*4)+(3*1)+(2*9)+(1*5)=87
87 % 10 = 7
So 941-95-7 is a valid CAS Registry Number.
941-95-7Relevant academic research and scientific papers
Studying the reactivity of (phthalazin-1(2H)-on-2-yl)methyl trichloroacetimidate towards different C- and O-nucleophiles
El Nezhawy, Ahmed O.H.,Gaballah, Samir T.,Radwan, Mohamed A.A.
body text, p. 6646 - 6650 (2010/03/01)
A simple and efficient synthesis of phthalazin-1(2H)-one 2-substituted derivatives is achieved in very good yields via reaction of a phthalazinone-trichloroacetimidate with various C- and O-nucleophiles such as aromatic, heteroaromatic and olefinic reagen