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Benzenamine, 4-methyl-N-[(4-nitrophenyl)methylene]-, also known as 4-methyl-N-(4-nitrobenzylidene)aniline or 4'-nitro-4-anisidine, is an organic compound with the chemical formula C14H14N2O2. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. Benzenamine, 4-methyl-N-[(4-nitrophenyl)methylene]- is primarily used as an intermediate in the synthesis of various dyes, pigments, and pharmaceuticals, including the production of azo dyes and certain anti-inflammatory drugs. It is also known for its potential applications in the field of materials science, particularly in the development of conductive polymers. Due to its reactivity and the presence of a nitro group, it is important to handle this chemical with care, as it may pose certain health and environmental risks.

730-39-2

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730-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 730-39-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 730-39:
(5*7)+(4*3)+(3*0)+(2*3)+(1*9)=62
62 % 10 = 2
So 730-39-2 is a valid CAS Registry Number.

730-39-2SDS

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 N-(4-methylphenyl)-1-(4-nitrophenyl)methanimine

1.2 Other means of identification

Product number -
Other names N-(4-nitro-benzylidene)-p-toluidine

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:730-39-2 SDS

730-39-2Relevant academic research and scientific papers

Synthesis of Green/Blue Light Emitting Quinolines by Aza-D-A Reaction Using InCl3 Catalyst

Singh, Rajkumar Romeshkumar,Singh, Thokchom Prasanta,Singh, Ningthoujam Premananda,Naorem, Shanta Singh,Singh, Okram Mukherjee

, p. 247 - 257 (2020/11/24)

An efficient InCl3-catalyzed sequential reaction of aromatic amines, aromatic aldehydes and functionalized alkynes leading to the formation of new quinoline derivatives exhibiting significant fluorescence activities is described. The photophysi

Observation of the complex spectra for the supramolecular system involving silver nanoparticles-biaryl Schiff bases containing the nitro group

Cao, Chao-Tun,Cheng, Shi-Mao,Cao, Chenzhong

, (2020/02/11)

A series of biaryl Schiff bases containing the nitro groups, 4-XArCH═NArNO2-4′ (XBANO2-4′) and 4-NO2ArCH═NArY-4′ (4-NO2BAY), were synthesized. Also, the fish sperm DNA (fsDNA) and silver nanoparticles (AgNPs) solutions were prepared. By mixing these compounds with fsDNA or AgNPs solution and determining the ultraviolet absorption spectra of the mixture solutions, an interesting phenomenon was found: a new absorption peak λmax,lim appeared in the (XBANO2-4′)-AgNPs solution, which was longer than the wavelength of λmax of XBANO2-4′ solution. The new absorption peak in the (XBANO2-4′)-AgNPs solution was the complex spectrum originating from the electron transfer between XBANO2-4′ and AgNPs. Whereas this phenomenon was not observed in the (4-NO2BAY)-AgNPs solutions, a quantitative correlation analysis was carried out with the measured spectral data, and the results show that the wave number νmax,lim of the λmax,lim is mainly affected by the excited-state substituent constant (Formula presented.) rather than the ground Hammett constant σ of the X group. The redshift magnitude Δνmax,WSL, namely, Δνmax,WSL = (1/λmax) ? (1/λmax,lim), of the wavelength λmax,lim is related to the highest occupied molecular orbital and lowest unoccupied molecular orbital of XBANO2-4′. The discovery of this new phenomenon is helpful to understanding the interaction between AgNPs-organic compound supramolecular systems.

Dehydrogenation and α-functionalization of secondary amines by visible-light-mediated catalysis

Bujok, Robert,Morawska, Paulina,Pawlowski, Robert,Stanek, Filip,Stodulski, Maciej

, p. 2103 - 2112 (2020/03/27)

A visible-light-mediated process for dehydrogenation of amines has been described. The given protocol showed a broad substrate scope, mild reaction conditions and excellent results without the requirement of tedious purification. This process can be applied in one-pot functionalization of secondary amines with various nucleophiles through the cooperation of visible-light and Lewis acid catalysis, leading to the structurally varied essential components of biologically active molecules. In addition, Stern-Volmer studies and quenching experiments revealed the role of a catalyst and led to the proposed mechanism of this transformation.

FeCl3-Mediated One-Pot Cyclization–Aromatization of Anilines, Benzaldehydes, and Phenylacetylenes under Ball Milling: A New Alternative for the Synthesis of 2,4-Diphenylquinolines

Tan, Ya-Jun,Wang, Fang-Jian,Asirib, Abdullah M.,Marwanib, Hadi M.,Zhang, Ze

, p. 65 - 73 (2017/10/11)

A straightforward and efficient method has been developed for the solvent-free synthesis of 2,4-diphenylquinolines via a one-pot reaction of anilines, benzaldehydes, and phenylacetylenes promoted by FeCl3 under solvent-free mechanochemical ball

Dual Heterogeneous Catalyst Pd-Au@Mn(II)-MOF for One-Pot Tandem Synthesis of Imines from Alcohols and Amines

Chen, Gong-Jun,Ma, Hui-Chao,Xin, Wen-Ling,Li, Xiao-Bo,Jin, Fa-Zheng,Wang, Jing-Si,Liu, Ming-Yang,Dong, Yu-Bin

supporting information, p. 654 - 660 (2017/01/13)

A new Mn(II) metal-organic framework (MOF) 1 was synthesized by the combination of 4,4,4-trifluoro-1-(4-(pyridin-4-yl)phenyl)butane-1,3-dione (L) and Mn(OAc)2 in solution. 1 features a threefold-interpenetrating NbO net containing honeycomb-like channels, in which the opposite Mn(II)···Mn(II) distance is 23.5075(10) ?. Furthermore, 1 can be an ideal platform to support Pd-Au bimetallic alloy nanoparticles to generate a composite catalytic system of Pd-Au@Mn(II)-MOF (2). 2 can be a highly active bifunctional heterogeneous catalyst for the one-pot tandem synthesis of imines from benzyl alcohols and anilines and from benzyl alcohols and benzylamines.

Azetidinone derivatives and its preparation method and application

-

Paragraph 0061; 0062, (2017/03/28)

The invention discloses azacyclobutanone derivatives which are compounds as shown in the formula (I) and medicinal salts thereof. The invention further discloses a preparation method and application of the azacyclobutanone derivatives. The azacyclobutanone derivatives disclosed by the invention can be used for treating or preventing atherosclerosis or lowering plasma cholesterol level, and has strong plasma cholesterol reducing activity and wide market prospect.

Silver-catalyzed one-step synthesis of multiply substituted quinolines

Xu, Xuefeng,Liu, Wenmin,Wang, Zhiqiang,Feng, Yuquan,Yan, Yanlei,Zhang, Xu

supporting information, p. 226 - 229 (2015/12/31)

A silver-catalyzed formation of C-C bond for the construction of a series of polysubstituted quinolines from arylamines, aldehydes, and ketones or arylamines and 1,3-diketones has been developed. The transformation is effective for a broad range of substrates, thus enabling the expansion of constituent architectures on the heterocyclic framework. This use of a single catalytic system to mediate chemical transformations in a synthetic operation is important for the development of new atom-economic strategies and this strategy is efficient in building complex structures from simple starting materials in an environmentally benign fashion.

Effective catalysis of imine metathesis by means of fast transiminations between aromatic-aromatic or aromatic-aliphatic amines

Ciaccia, Maria,Pilati, Silvia,Cacciapaglia, Roberta,Mandolini, Luigi,Di Stefano, Stefano

, p. 3282 - 3287 (2014/05/06)

This paper reports on a quantitative investigation of rates of amine-imine exchange reactions of primary amines with their benzylidene derivatives in organic solvents at room temperature. Exchange reactions involving aromatic-aromatic or aromatic-aliphati

Morphology-tuned exceptional catalytic activity of porous-polymer-supported Mn3O4 in aerobic sp3 C-H bond oxidation of aromatic hydrocarbons and alcohols

Mondal, John,Borah, Parijat,Sreejith, Sivaramapanicker,Nguyen, Kim Truc,Han, Xiguang,Ma, Xing,Zhao, Yanli

, p. 3518 - 3529 (2015/04/16)

Mn3O4 nanomaterials with different morphologies (sphere, nanowire, and octahedron) embedded into functionalized nanoporous polymers were developed by a facile one-pot solvothermal technique at different temperatures. These Mn3O4-based hybrid materials could behave as heterogeneous nanocatalysts to perform sp3 C-H bond oxidation of aromatic hydrocarbons and alcohols with molecular oxygen as an economic oxidant. Catalytic activity could be effectively tuned by changing the morphology of incorporated Mn3O4 in nanoporous polymer. These Mn3O4-based hybrid materials exhibited remarkable catalytic performance for sp3 C-H bond oxidation as compared with bare Mn3O4 nanoparticles. Mn3O4 with octahedral morphology in nanoporous polymer exhibited the highest catalytic activity on account of its more exposed crystallographic planes and edges. These Mn3O4-based nanocatalysts could be recycled and reused for consecutive catalytic cycles without a significant loss of catalytic activity. Exceptional crystal facets: Nanoporous-polymer-supported Mn3O4 nanocatalysts (Mn@DVTA, DVTA=divinyltriallyl) with different morphologies are developed to catalyze aerobic sp3 C-H bond oxidation of aromatic hydrocarbons and alcohols. Among the different nanocatalysts, those with octahedral crystallite morphology exhibit outstanding catalytic performance.

Synthesis of 4-imino-2H,3H,5H-[1,2,5]thiadiazolidin-1-oxide through cycloaddition reaction of N-sulphinylanilines and N-(α-cyano-α-aryl) -methylanilines

Kaur, Manpreet,Singh, Baldev

, p. 1157 - 1161 (2014/08/05)

Through the normal mode of cycloaddition reaction of N-(α-cyano- α-aryl)-methylanilines (II) onto N-sulphinylanilines (III) has provided 2,3,5-triaryl-4-imino-2H,3H,5H-[1,2,5]thiadiazolidin-1-oxides (IV). The present protocol has advantage of convenient operation to synthesize heterocyclics in good yield.

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