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4-(3-nitrophenyl)-2-oxobut-3-enoic acid is a chemical compound with the molecular formula C10H7NO5. It is an organic molecule that features a 3-nitrophenyl group attached to a 2-oxobut-3-enoic acid moiety. 4-(3-nitrophenyl)-2-oxobut-3-enoic acid is characterized by a conjugated diene system, which includes a carbonyl group and a nitro group, providing it with unique chemical properties. It is often used in the synthesis of various pharmaceuticals and other organic compounds due to its reactive nature and the presence of functional groups that can participate in a range of chemical reactions. The compound's structure allows for potential applications in the development of new drugs, agrochemicals, and other specialty chemicals, making it a subject of interest in the field of organic chemistry.

1772-65-2

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1772-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1772-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1772-65:
(6*1)+(5*7)+(4*7)+(3*2)+(2*6)+(1*5)=92
92 % 10 = 2
So 1772-65-2 is a valid CAS Registry Number.

1772-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-nitrophenyl)-2-oxobut-3-enoic acid

1.2 Other means of identification

Product number -
Other names 4t-(2,6,6-trimethyl-cyclohex-1-enyl)-but-3-en-2-one thiosemicarbazone

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:1772-65-2 SDS

1772-65-2Relevant academic research and scientific papers

Crystal Engineering of 6-Carboxy-4-aryl-2,2′-bipyridine Complexes: Potent Chelators with Intrinsic Intermolecular Affinity

Dalton, Hannah L.,Hawes, Chris S.,Gunnlaugsson, Thorfinnur

, p. 4365 - 4376 (2017)

Herein we report the coordination chemistry and structural properties of two multifunctional terdentate 2,2′-bipyridine derivatives 4- and 3-(4-nitrophenyl)-2,2′-bipyridine-6-carboxylate, L1/L2, respectively. We report eight new coordination complexes wit

Synthesis, Characterization, and Biological Profiling of Ruthenium(II)-Based 4-Nitro- And 4-Amino-1,8-naphthalimide Conjugates

Elmes, Robert B. P.,Erby, Maria Luisa,Frimannsson, Daniel O.,Gunnlaugsson, Thorfinnur,Kitchen, Jonathan A.,Lawler, Mark,Quinn, Susan J.,Ryan, Gary J.,Williams, D. Clive

supporting information, (2020/07/27)

We report the synthesis, photophysical characterization, and biological evaluation of four DNA-binding ruthenium(II) polypyridyl 4-nitro- and 4-amino-1,8-naphthalimide conjugates. A meta arrangement around the ring connecting the 1,8-naphthalimide to a bipyridine ligand creates a cleft, the result of which renders the shape of the complex complementary to that of DNA. We have demonstrated that each complex exhibits water solubility and a distinctive set of photophysical properties that has allowed the nature of their interaction with DNA to be probed by various ground- and excited-state titrations. Furthermore, by varying the ancillary ligands, we also demonstrate their ability to act as DNA photocleavers, where all compounds have been found to cleave supercoiled DNA with high efficiency. Detailed cellular uptake experiments revealed that the conjugates accumulate in the cytoplasm and nucleus of HeLa cells, showing characteristic red metal-to-ligand charge-transfer emission, and also exhibit photoactivated cytotoxicity within the cells upon irradiation at 450 nm. A comparison between the meta and para arrangements of the 1,8-naphthalimide moiety relative to the Ru(II) center suggests increased DNA binding in the case of the meta arrangement; however, bipyridine-4-amino-1,8-naphthalimide conjugates appear to show superior phototoxicity in comparison to their 4-nitro derivatives.

Functionalisation of gold nanoparticles with ruthenium(ii) polypyridyl complexes for their application in cellular imaging

Dalton, Hannah L.,Estalayo-Adrián, Sandra,Gunnlaugsson, Thorfinnur,Kelly, John M.,McManus, Gavin J.,Savyasachi, Aramballi J.

, p. 14158 - 14168 (2020/11/02)

Two new dinuclear Ru(ii) polypyridyl complexes containing an alkyl disulphide functionalised bipyridine-based ligand and either 1,10-phenanthroline (phen) or 1,4,5,8-tetraazaphenanthrene (TAP) as ancillary ligands have been synthesised and characterised. Their attachment onto the surface of gold nanoparticles (AuNPs, average diameter of ca. 2.5 nm) resulted in the formation of two new water-soluble Ru(ii)-AuNP conjugates that combine the advantageous properties of both moieties. Both free complexes show the attractive photophysical properties of Ru(ii) polypyridyl complexes and a rapid cellular uptake in HeLa cervical cancer cells. However, their corresponding gold conjugates displayed lower quantum yields than those determined for the free complexes presumed to be due to an energy transfer quenching of the Ru(ii) luminescence by interaction with the gold surface. Despite their diminished luminescence, confocal fluorescence microscopy studies revealed that the Ru(ii)-AuNP conjugates are successfully internalised into HeLa cells and better tolerated than their free complex counterparts after 24 h incubation, which makes them potential luminescent nanomaterials for bioimaging applications.

Ag/CdS nanocomposite: An efficient recyclable catalyst for the synthesis of novel 8-aryl-8h-[1,3]dioxolo[4,5-g]chromene-6-carboxylic acids under mild reaction conditions

Abdolmohammadi, Shahrzad,Nasrabadi, Seyed Reza Rasouli,Seif, Ahmad,Fard, Narges Elmi

, p. 323 - 328 (2018/08/10)

Aim and Objective: Chromene derivatives are privileged heterocyclic systems that exhibit various types of biological properties such as antioxidant, anticancer, antimicrobial, hypotensive, and local anesthetic. Cadmium sulfide nanoparticles (CdS NPs) as an efficient heterogeneous catalyst is used in various organic transformations because of its certain unique and unusual physico-chemical properties. The effectiveness of catalytic activity of CdS NPs can be improved due to the combined effect of Ag particles. Results: Ag/CdS nanocomposite is a readily available, recyclable, and non-toxic catalyst used for the highly efficient synthesis of novel 8-aryl-8H-[1,3]dioxolo[4,5-g]chromrne-6-carboxylic acids. This reaction is conveniently performed under mild reaction conditions. All synthesized compounds were well characterized by their satisfactory elemental analyses, IR, 1H and 13C NMR spectroscopy. The synthesized catalyst was fully characterized by XRD, SEM, and EDX techniques. Materials and Methods: The present methodology focuses on the condensation reaction of arylmethylidenepyruvic acids with 3,4-methylenedioxyphenol, using a catalytic amount of Ag/CdS nanocomposite (15 mol%) in aqueous media at room temperature to afford 8-aryl-8H-[1,3]dioxolo [4,5-g]chromrne-6-carboxylic acids in high yields (90-97%) within short reaction times (2-4 h). The Ag/CdS nanocomposite was also prepared by an ultrasonic-assisted sol-gel method. Conclusion: In conclusion, we have successfully synthesized novel 8-aryl-8H-[1,3]dioxolo[4,5- g]chromrne-6-carboxylic acid derivatives by the Ag/CdS nanocomposite catalyzed cyclocondensation reaction of arylmethylidenepyruvic acids with 3,4-methylenedioxyphenol under mild reaction conditions. Environmentally benign procedure, high to excellent yields of products, simplicity of operation, and use of readily available and recyclable catalyst are the advantages of this new practical reaction.

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