736-31-2 Usage
Description
(E)-1,1'-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE), also known as 1,2-bis(4-nitrophenyl)ethene, is a chemical compound with the molecular formula C14H10N4O4. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. (E)-1,1′-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE) is known for its potential applications in various fields, including organic synthesis, pharmaceuticals, and agrochemicals.
Uses
Used in Organic Synthesis:
(E)-1,1'-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE) is used as an intermediate in the synthesis of various organic compounds and dyes. Its unique structure allows it to be a valuable building block for creating a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E)-1,1'-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE) is used as a key component in the production of certain drugs. Its properties make it suitable for the development of new pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Industry:
(E)-1,1'-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE) also finds application in the agrochemical industry, where it is utilized in the development of pesticides and other agricultural chemicals. Its chemical properties contribute to the effectiveness of these products in protecting crops and enhancing agricultural productivity.
Used in Materials Science:
(E)-1,1'-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE) may have potential applications in the field of materials science, particularly in the development of new functional materials. Its unique properties could be harnessed to create innovative materials with specific characteristics for various applications.
Safety Precautions:
It is important to handle (E)-1,1'-(1,2-ETHENEDIYL)BIS(4-NITROBENZENE) with care, as it is toxic and can cause irritation to the skin, eyes, and respiratory system. Proper safety measures, including the use of personal protective equipment and proper ventilation, should be taken to minimize the risk of exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 736-31-2 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 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 736-31:
(5*7)+(4*3)+(3*6)+(2*3)+(1*1)=72
72 % 10 = 2
So 736-31-2 is a valid CAS Registry Number.
736-31-2Relevant articles and documents
Fouad,Farrell
, p. 3881 (1975)
Single-molecule conductance in a unique cross-conjugated tetra(aminoaryl)ethene
Medina Rivero, Samara,García Arroyo, Paloma,Li, Liang,Gunasekaran, Suman,Stuyver, Thijs,Manche?o, María José,Alonso, Mercedes,Venkataraman, Latha,Segura, José L.,Casado, Juan
supporting information, p. 591 - 594 (2021/01/29)
A 1,1,2,2-tetrakis(4-aminophenyl)ethene with three paths of π-conjugation, linear-cis, linear-trans and a cross-conjugation, has been prepared. The molecule is able to bind to gold electrodes forming molecular junctions for single-molecule conductance measurements. Only two regimes of conduction are found experimentally. The modelling of the conductance allows to assign them to through-bond transmission in the linear case, while the cross-conjugated channel is further assisted by through-space transmission, partially alleviating the destructive quantum interference. This journal is
Second-generation aryl isonitrile compounds targeting multidrug-resistant Staphylococcus aureus
Kyei-Baffour, Kwaku,Mohammad, Haroon,Seleem, Mohamed N.,Dai, Mingji
supporting information, p. 1845 - 1854 (2019/03/28)
Antibiotic resistance remains a major global public health threat that requires sustained discovery of novel antibacterial agents with unexploited scaffolds. Structure-activity relationship of the first-generation aryl isonitrile compounds we synthesized led to an initial lead molecule that informed the synthesis of a second-generation of aryl isonitriles. From this new series of 20 compounds, three analogues inhibited growth of methicillin-resistant Staphylococcus aureus (MRSA) (from 1 to 4 μM) and were safe to human keratinocytes. Compound 19, with an additional isonitrile group exhibited improved activity against MRSA compared to the first-generation lead compound. This compound emerged as a candidate worthy of further investigation and further reinforced the importance of the isonitrile functionality in the compounds’ anti-MRSA activity. In a murine skin wound model, 19 significantly reduced the burden of MRSA, similar to the antibiotic fusidic acid. In summary, 19 was identified as a new lead aryl isonitrile compound effective against MRSA.