5466-93-3 Usage
Description
N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is a chemical compound with the molecular formula C12H16N2O4. It is an ethyl ester derivative of N-(4-aminophenyl)carbamic acid, known for its potential antimicrobial, antifungal properties, and enzyme inhibitory activity. N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is frequently utilized in organic synthesis and pharmaceutical research, with ongoing investigations into its applications in drug development and therapy for various medical conditions.
Uses
Used in Pharmaceutical Research:
N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is used as a research compound for its potential antimicrobial and antifungal properties, serving as a foundation for developing new treatments against infectious diseases.
Used in Organic Synthesis:
In the field of organic synthesis, N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is used as an intermediate or reactant in the synthesis of more complex organic molecules, contributing to the creation of novel chemical entities.
Used in Enzyme Inhibition Studies:
N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester is also used as a potential enzyme inhibitor, playing a role in studies aimed at understanding and manipulating enzyme activity for therapeutic benefits.
Used in Drug Development:
N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester may have applications in the development of new drugs and therapies for various medical conditions, although further research is required to fully explore its potential and side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 5466-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5466-93:
(6*5)+(5*4)+(4*6)+(3*6)+(2*9)+(1*3)=113
113 % 10 = 3
So 5466-93-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O4/c1-3-17-11(15)13-9-5-7-10(8-6-9)14-12(16)18-4-2/h5-8H,3-4H2,1-2H3,(H,13,15)(H,14,16)
5466-93-3Relevant articles and documents
Sustainable Carboxylation of Diamines with Hydrogen Carbonate
Forte, Gianpiero,Chiarotto, Isabella,Richter, Frank,Trieu, Vinh,Feroci, Marta
, p. 1323 - 1327 (2018/09/21)
A protocol for the carboxylation of diamines employing quaternary ammonium hydrogen carbonates as C1 source is presented. The approach is used to obtain industrially relevant bis-O-alkyl carbamates with diverse structural features in very high yield, even on gram scale. The quaternary ammonium salts, formally acting as "transporters" of the carboxylating agent, can be recovered after the reaction, and recycled with high efficiency. Regeneration of the hydrogen carbonates on ion-exchange resin grants excellent atom economy in the process.
New metal complexes of semicarbazones derived from para phenylene diamine of NOO/or NO donor sites and their antimicrobial screening
Saleh,Eid,Khalil,El-Ghamry
experimental part, p. 337 - 356 (2010/04/02)
THE SYNTHESIS and characterization of new Mn(II). Co(II). Ni(II) and Cu(II) complexes with semicarbazone ligands derived from para phenylene diamine {where L1 = Semicarbazide-4-yl-benzene-4 (2-hydroxybenzalde-hydc semicarbazone) [SBHBS], L
A new access to quinazolines from simple anilines
Chilin, Adriana,Marzaro, Giovanni,Zanatta, Samuele,Barbieri, Vera,Pastorini, Giovanni,Manzini, Paolo,Guiotto, Adriano
, p. 12351 - 12356 (2007/10/03)
A new synthetic pathway to quinazolines is described. This new method uses hexamethylenetetramine in TFA and potassium ferricyanide in aqueous ethanolic KOH, starting from simple N-protected anilines. The method affords substituted quinazolines with high
