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1-[(4-fluorophenyl)hydrazono]naphthalen-2(1H)-one is a complex organic compound characterized by a naphthalen-2(1H)-one core, which features a naphthalene ring with a carbonyl group at position 2 and a hydrogen atom at position 1. The molecule is further distinguished by the presence of a hydrazone functional group, which is formed by the condensation of a hydrazine with a carbonyl group. In this specific compound, the hydrazone is linked to a 4-fluorophenyl group, indicating that one of the hydrogen atoms on the phenyl ring is replaced by a fluorine atom. This substitution can significantly alter the chemical and physical properties of the molecule, potentially affecting its reactivity, stability, and interaction with other molecules. The compound may be of interest in various fields, such as pharmaceuticals, materials science, or as a precursor in organic synthesis, due to its unique structure and potential applications.

1960-13-0

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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.

1960-13-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z)-1-[(4-fluorophenyl)hydrazinylidene]naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 1-(4-Fluor-benzolazo)-naphthol-(2)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1960-13-0 SDS

1960-13-0Downstream Products

1960-13-0Relevant academic research and scientific papers

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.

An environmentally friendly approach to the green synthesis of azo dyes with aryltriazenes via ionic liquid promoted C-N bonds formation

Zhang, Yonghong,Liu, Yonghong,Ma, Xiaoqian,Ma, Xia,Wang, Bin,Li, Hongguang,Huang, Yan,Liu, Chenjiang

, p. 438 - 444 (2018/06/14)

An efficient and green approach for the synthesis of azo dyes has been developed via the Br?nsted acidic ionic liquid (IL) promoted diazo coupling reaction of naphthols with aryltriazenes. The reaction was carried out with the aryltriazenes as diazotizing

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.

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