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N-[[2-(phenylhydrazinylidene)acenaphthen-1-ylidene]amino]aniline is a complex organic compound with the molecular formula C26H19N3. It is characterized by a phenylhydrazine group attached to an acenaphthene moiety, which is then linked to an aniline group. N-[[2-(phenylhydrazinylidene)acenaphthen-1-ylidene]amino]aniline is known for its potential applications in chemical research and as an intermediate in the synthesis of various pharmaceuticals and dyes. Its structure features a conjugated system of double bonds and aromatic rings, which can contribute to its chemical reactivity and stability. The compound's specific properties and reactivity make it a subject of interest in the field of organic chemistry, particularly for its potential roles in the development of new materials and compounds.

1932-06-5

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1932-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1932-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1932-06:
(6*1)+(5*9)+(4*3)+(3*2)+(2*0)+(1*6)=75
75 % 10 = 5
So 1932-06-5 is a valid CAS Registry Number.

1932-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[2-(phenylhydrazinylidene)acenaphthylen-1-ylidene]amino]aniline

1.2 Other means of identification

Product number -
Other names Acenaphthen-1,2-dion-bis-phenylhydrazon

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:1932-06-5 SDS

1932-06-5Relevant academic research and scientific papers

Experimental and theoretical study on spontaneous intermolecular charge transfer features and antiaromaticities of unusual bisazo compounds with antiaromatic cores

Zhang, Yun-Fan,Zhang, Chao-Zhi

, p. 225 - 232 (2019)

Antiaromatic compounds have been applied in optoelectronic devices. In this paper, acenaphthoquinone bisphenylhydrazone (1a) and acenaphthoquinone bis(4-bromophenylhydrazone) (2a), were synthesized by a Schiff base reaction of acenaphthoquinone with pheny

Effect of bromine substituent on optical properties of aryl compounds

Zhang, Chao-Zhi,Li, Ting,Yuan, Yang,Gu, Cheng-Yue,Niu, Meng-Xiao,Cao, Hui

, (2017/04/13)

Substituents significantly affect optical properties of organic compounds. In this study, a series of organic compounds were synthesized. Ultraviolet-visible and cyclic voltammetry spectra were determined. The relationships between the number of π electron in an aryl ring and the redshift (and molecular orbital energy levels) were studied. To investigate mechanisms of the bromine substituent effects, theoretical calculations were carried out. Ultraviolet-visible spectra of bromine-containing compounds exhibit obvious redshifts (0.04-0.17?eV) of the maximal absorption wavelengths and enhanced absorbance (11%-57%) compared with corresponding reference compounds. The lowest unoccupied and highest occupied molecular orbital energy levels of compounds containing bromine substituents are 0.05 to 0.60 and 0.02 to 0.40?eV lower than that of corresponding reference compounds. On the whole, the redshifts and the reduced molecular orbital energy levels caused by bromine substituent decrease with the increase in the number of π electron in an aryl ring. The effects would be attributed to strong p-π conjugation between p electron in the bromine substituent and π electrons in aryl rings. Therefore, this paper suggests a useful way for tuning optical absorption and molecular orbital energy levels of aryl compounds.

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