1960-13-0 Usage
Structure
Naphthalen-2(1H)-one with a hydrazono substituent at the 1-position and a 4-fluorophenyl group attached to the hydrazone nitrogen
Potential applications
Organic synthesis and medicinal chemistry
Unique structure
The presence of the hydrazono and 4-fluorophenyl groups may contribute to its potential reactivity and pharmaceutical properties
Precursors
May be used as a precursor for the synthesis of other organic compounds
Pharmaceutical properties
May have potential pharmaceutical properties, but further research is necessary to fully understand its chemical and biological properties
Research necessity
Additional research is needed to explore the full potential of 1-[(4-fluorophenyl)hydrazono]naphthalen-2(1H)-one in various applications
Check Digit Verification of cas no
The CAS Registry Mumber 1960-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1960-13:
(6*1)+(5*9)+(4*6)+(3*0)+(2*1)+(1*3)=80
80 % 10 = 0
So 1960-13-0 is a valid CAS Registry Number.
1960-13-0Relevant articles and documents
One-pot synthesis of azo compounds in the absence of acidic or alkaline additives
Cheng, Xin-Wang,Duan, Pan,Liu, Ting-Ting,Yan, Jiao-Zhao,Zeng, Yao-Fu
, p. 486 - 490 (2020/10/22)
A one-pot method for the synthesis of azo compounds by the reaction of β-naphthol with aryl amines using t-BuONO as the nitrosonium source in DCM at room temperature was developed. This method features mild reaction conditions, a simple experimental procedure, and is free of acidic or alkaline additives.
Fe(HSO4)3 as an Efficient Catalyst for Diazotization and Diazo Coupling Reactions
Rahimizadeh, Mohammad,Eshghi, Hossein,Shiri, Ali,Ghadamyari, Zohreh,Matin, Maryam M.,Oroojalian, Fatemeh,Pordeli, Parvaneh
, p. 716 - 719 (2013/05/08)
Diazo coupling reactions of aromatic amines with 2-naphthol in a green, efficient and easy procedure is described. Ferric hydrogensulfate catalyses this reaction in water at room temperature and short reaction time with high yields. The antibacterial activities of the synthesized compounds against four pathogenic bacteria are also investigated.
