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Carbamic acid, [4-(chlorocarbonyl)phenyl]-, ethyl ester, also known as ethyl 4-(chlorocarbonyl)phenylcarbamate, is an organic compound with the chemical formula C10H10ClNO3. It is a derivative of carbamic acid, featuring a chlorocarbonyl group attached to a phenyl ring and an ethyl ester group. Carbamic acid, [4-(chlorocarbonyl)phenyl]-, ethyl ester is primarily used as an intermediate in the synthesis of various agrochemicals, particularly herbicides and pesticides. Due to its reactivity and potential toxicity, it is important to handle this chemical with care and in accordance with safety regulations.

5180-74-5

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5180-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5180-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5180-74:
(6*5)+(5*1)+(4*8)+(3*0)+(2*7)+(1*4)=85
85 % 10 = 5
So 5180-74-5 is a valid CAS Registry Number.

5180-74-5Relevant academic research and scientific papers

An integrative study to identify novel scaffolds for sphingosine kinase 1 inhibitors

Vettorazzi, Marcela,Angelina, Emilio,Lima, Santiago,Gonec, Tomas,Otevrel, Jan,Marvanova, Pavlina,Padrtova, Tereza,Mokry, Petr,Bobal, Pavel,Acosta, Lina M.,Palma, Alirio,Cobo, Justo,Bobalova, Janette,Csollei, Jozef,Malik, Ivan,Alvarez, Sergio,Spiegel, Sarah,Jampilek, Josef,Enriz, Ricardo D.

, p. 461 - 481 (2017/08/21)

Sphingosine kinase 1 (SphK1), the enzyme that produces the bioactive sphingolipid metabolite, sphingosine-1-phosphate, is a promising new molecular target for therapeutic intervention in cancer and inflammatory diseases. In view of its importance, the main objective of this work was to find new and more potent inhibitors for this enzyme possessing different structural scaffolds than those of the known inhibitors. Our theoretical and experimental study has allowed us to identify two new structural scaffolds (three new compounds), which could be used as starting structures for the design and then the development of new inhibitors of SphK1. Our study was carried out in different steps: virtual screening, synthesis, bioassays and molecular modelling. From our results, we propose a new dihydrobenzo[b]pyrimido[5,4-f]azepine and two alkyl{3-/4-[1-hydroxy-2-(4-arylpiperazin-1-yl)ethyl]phenyl}carbamates as initial structures for the development of new inhibitors. In addition, our molecular modelling study using QTAIM calculations, allowed us to describe in detail the molecular interactions that stabilize the different Ligand-Receptor complexes. Such analyses indicate that the cationic head of the different compounds must be refined in order to obtain an increase in the binding affinity of these ligands.

Synthesis, analysis, cholinesterase-inhibiting activity and molecular modelling studies of 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxy-carbonyl)amino]benzoates and their quaternary ammonium salts

Padrtova, Tereza,Marvanova, Pavlina,Odehnalova, Klara,Kubinova, Renata,Parravicini, Oscar,Garro, Adriana,Enriz, Ricardo D.,Humpa, Otakar,Oravec, Michal,Mokry, Petr

, (2017/12/05)

Tertiary amines 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxycarbonyl)amino]benzoates and their quaternary ammonium salts were synthesized. The final step of synthesis of quaternary ammonium salts was carried out by microwave-assisted synthesis. Software-ca

Synthesis and pharmacological evaluation of novel potential ultrashort-acting β-blockers

Mokry,Zemanova,Csoellei,Racanska,Tumova

, p. 18 - 21 (2007/10/03)

The basic relationship between chemical structure and pharmacological activity of eight newly developed potential ultrashort-acting β-adrenergic blockers was evaluated. The compounds studied are derivatives of arylcarbonyloxyaminopropanols and were prepar

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