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(4''-NITRO-1,1':4',1''-TERPHENYL-4-YL)AMINE, also known as NNTA, is a chemical compound characterized by a terphenyl core with a nitro group at the 4th position and an amine group attached at the 4'' position. It is recognized for its distinctive structure and is widely utilized in research and development as a fundamental building block for the synthesis of a variety of organic compounds. NNTA's properties and reactivity contribute to its value in the design and creation of innovative chemical compounds, with potential applications spanning materials science, pharmaceuticals, and organic electronics. However, due to its toxic and potentially harmful nature, it is crucial to handle NNTA with appropriate safety measures.

38190-45-3

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38190-45-3 Usage

Uses

Used in Research and Development:
NNTA is used as a building block in the synthesis of various organic compounds for research and development purposes. Its unique structure and reactivity make it a valuable tool in the creation of new chemical entities.
Used in Materials Science:
In the field of materials science, NNTA is used as a component in the development of advanced materials due to its structural and chemical properties that can contribute to the desired material characteristics.
Used in Pharmaceuticals:
NNTA is utilized as a precursor or intermediate in the synthesis of pharmaceutical compounds, potentially leading to the discovery of new drugs or drug candidates.
Used in Organic Electronics:
NNTA is employed in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) or organic photovoltaics, where its chemical properties can enhance device performance.
Used in Chemical Synthesis:
NNTA is used as a reagent in various chemical synthesis processes, enabling the production of a range of chemical products with specific applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 38190-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,9 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38190-45:
(7*3)+(6*8)+(5*1)+(4*9)+(3*0)+(2*4)+(1*5)=123
123 % 10 = 3
So 38190-45-3 is a valid CAS Registry Number.

38190-45-3SDS

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 4-[4-(4-nitrophenyl)phenyl]aniline

1.2 Other means of identification

Product number -
Other names (4''-nitro-1,1':4',1''-terphenyl-4-yl)amine

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:38190-45-3 SDS

38190-45-3Downstream Products

38190-45-3Relevant academic research and scientific papers

Azo bond formation on metal surfaces

Meng, Xiangzhi,Klaasen, Henning,Viergutz, Lena,Schulze Lammers, Bertram,Witteler, Melanie C.,M?nig, Harry,Amirjalayer, Saeed,Liu, Lacheng,Neugebauer, Johannes,Gao, Hong-Ying,Studer, Armido,Fuchs, Harald

, p. 1458 - 1464 (2020/12/14)

The formation of azo compounds via redox cross-coupling of nitroarenes and arylamines, challenging in solution phase chemistry, is achieved by on-surface chemistry. Reaction products are analyzed with a cryogenic scanning tunneling microscope (STM) and X-ray photoelectron spectroscopy (XPS). By using well-designed precursors containing both an amino and a nitro functionality, azo polymers are prepared on surface via highly efficient nitro-amino cross-coupling. Experiments conducted on other substrates and surface orientations reveal that the metal surface has a significant effect on the reaction efficiency. The reaction was further found to proceed from partially oxidized/reduced precursors in dimerization reactions, shedding light on the mechanism that was studied by DFT calculations.

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