941-95-7 Usage
Heterocyclic compound
Phthalazine ring This compound 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 This compound 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 articles and documents
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
