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4-[(1-oxo-3,4-dihydronaphthalen-2-ylidene)methyl]benzonitrile, also known as BZN, is a chemical compound with the molecular formula C20H13NO. It is a yellowish solid that is insoluble in water but soluble in organic solvents. BZN is a versatile chemical with applications in both organic synthesis and potential biological activities.

68434-51-5

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68434-51-5 Usage

Uses

Used in Organic Synthesis:
4-[(1-oxo-3,4-dihydronaphthalen-2-ylidene)methyl]benzonitrile is used as a reagent in organic synthesis for the preparation of various aromatic compounds. Its unique structure allows for the formation of diverse organic molecules, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Biological Activities:
4-[(1-oxo-3,4-dihydronaphthalen-2-ylidene)methyl]benzonitrile has been studied for its potential biological activities, including antimicrobial and antioxidant properties. Its antimicrobial properties make it a candidate for use in the development of new antimicrobial agents to combat drug-resistant bacteria. Additionally, its antioxidant properties suggest potential applications in the prevention of oxidative stress-related diseases.
However, it is important to consider the potential toxicological effects and environmental impact of 4-[(1-oxo-3,4-dihydronaphthalen-2-ylidene)methyl]benzonitrile when handling and using 4-[(1-oxo-3,4-dihydronaphthalen-2-ylidene)methyl]benzonitrile. Further research is needed to fully understand its safety profile and optimize its applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 68434-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,3 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68434-51:
(7*6)+(6*8)+(5*4)+(4*3)+(3*4)+(2*5)+(1*1)=145
145 % 10 = 5
So 68434-51-5 is a valid CAS Registry Number.

68434-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(1-oxo-3,4-dihydronaphthalen-2-ylidene)methyl]benzonitrile

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:68434-51-5 SDS

68434-51-5Downstream Products

68434-51-5Relevant academic research and scientific papers

Ash of pomegranate peels (APP): A bio-waste heterogeneous catalyst for sustainable synthesis of α,α′-bis(substituted benzylidine)cycloalkanones and 2-arylidene-1-tetralones

Patil, Rupesh C.,Patil, Uttam P.,Jagdale, Ashutosh A.,Shinde, Sachinkumar K.,Patil, Suresh S.

, p. 3527 - 3543 (2020/05/13)

Abstract: α,α′-bis(substituted benzylidene)cycloalkanones were efficiently prepared from variously substituted aldehydes and cycloalkanones in water by using ash of pomegranate peels (APP) as a catalyst. The APP-catalyst was obtained from bio-waste by simple thermal treatment to dry peels of pomegranate fruit and formation of its active phase was confirmed by FT-IR, XRD, XRF, EDX, SEM, DSC-TGA and BET techniques. The analysis revealed that the present catalyst has basic sites which promote the synthesis of desired products. The main attractions of our protocol are utilization of highly abundant bio-waste-derived catalyst and good-to-excellent yield in shortest reaction time. This green protocol was further extended for structurally diverse 2-arylidene-1-tetralones by condensation of equimolar quantity of aromatic aldehydes and 1-tetralone at low temperature. The catalyst could be quantitatively recovered and reused effectively for five times. Graphic abstract: [Figure not available: see fulltext.].

UV-light induced domino type reactions: Synthesis and photophysical properties of unreported nitrogen ring junction quinazolines

Palaniraja, Jeyakannu,Roopan, Selvaraj Mohana

, p. 37415 - 37423 (2015/05/20)

An expedient method for the synthesis of 5,6-dihydrobenzo[h][1,2,4]triazolo[5,1-b]quinazolines by UV light has been developed. Our aim was to synthesize various α, β-unsaturated carbonyl compounds and to further react them with different amines in DMF, in

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