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Details

Stereochemistry ACHIRAL
Molecular Formula C3H6N2O
Molecular Weight 86.0925
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IMIDAZOLIDINONE

SMILES

O=C1NCCN1

InChI

InChIKey=YAMHXTCMCPHKLN-UHFFFAOYSA-N
InChI=1S/C3H6N2O/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)

HIDE SMILES / InChI

Molecular Formula C3H6N2O
Molecular Weight 86.0925
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bis(1,3-dimethyl-1,3-diazinan-2-one)dinitratodioxidouranium(VI).
2010-12-04
Computational thermochemistry of six ureas, imidazolidin-2-one, N,N'-trimethyleneurea, benzimidazolinone, parabanic acid, barbital (5,5'-diethylbarbituric acid), and 3,4,4'-trichlorocarbanilide, with an extension to related compounds.
2010-09-02
Bis[2-(ethoxy-carbonyl-amino)ethan-aminium] hexa-bromidostannate.
2009-11-11
trans-4,5-Dihydr-oxy-1,3-bis-(4-methoxy-phen-yl)imidazolidine-2-thione.
2009-10-23
trans-4,5-Dihydr-oxy-1,3-diphenyl-imidazolidine-2-thione.
2009-09-09
Gold(I)-catalyzed intramolecular dihydroamination of allenes with N,N'-disubstituted ureas to form bicyclic imidazolidin-2-ones.
2009-06-18
Photophysics and dihedral freedom of the chromophore in yellow, blue, and green fluorescent protein.
2009-01-08
Design, synthesis, and structure-activity relationships of novel insulin receptor tyrosine kinase activators.
2008-10-09
Synthesis and immunosuppressive activity evaluation of substituted N-imidazolidin-2-ones and N-tetrahydropyrimidin-2(1H)-ones.
2008-10
Stereoselective synthesis of quaternary center bearing azetines and their beta-amino acid derivatives.
2008-02-15
Selective androgen receptor modulators in preclinical and clinical development.
2008
Phenanthroline-derived ratiometric chemosensor for ureas.
2007-03-30
A new synthesis of imidazolidin-2-ones via Pd-catalyzed carboamination of N-allylureas.
2006-06-08
Potent inhibitors of the HIV-1 protease incorporating cyclic urea P1-P2 scaffold.
2004-11-15
A two-unnatural-base-pair system toward the expansion of the genetic code.
2004-10-20
Dichlorobis(imidazolidin-2-one-kappaO)zinc(II) at 150 K.
2003-11
Synthesis and antileishmanial activity of new imidazolidin-2-one derivatives.
2003-08-23
Methyl 2-(2-chloroethylaminocarbonyl)diazenecarboxylate SB-166 inhibits the growth of different tumour cell lines, including drug-resistant sublines.
2003-04
[A novel and practical synthesis of (+)-biotin via Fukuyama coupling reaction].
2003-02
In vitro and in vivo antileishmanial activity of 2-amino-4,6-dimethylpyridine derivatives against Leishmania mexicana.
2002-12
Kinetics and mechanism for CO(2) scrambling in a N-carboxyimidazolidone analogue for N(1)-carboxybiotin.
2002-09-25
Further insight in the photochemistry of DNA: structure of a 2-imidazolone (5-4) pyrimidone adduct derived from the mutagenic pyrimidine (6-4) pyrimidone photolesion by UV irradiation.
2002-03-20
Domino reactions of amidines with methyl 2-chloro-2-cyclopropylideneacetate as an efficient access to cyclobutene-annelated pyrimidinones.
2002-03-07
Interaction of biotin with Mg-O bonds: bifunctional binding and recognition of biotin and related ligands by the Mg(15-crown-5)2+ unit.
2002-03-06
Novel 1,4-diphosphanes with imidazolidin-2-one backbones as chiral ligands: highly enantioselective Rh-catalyzed hydrogenation of enamides.
2002-03-01
Catalytic asymmetric intramolecular aminopalladation: enantioselective synthesis of vinyl-substituted 2-oxazolidinones, 2-imidazolidinones, and 2-pyrrolidinones.
2002-01-09
An unnatural base pair between imidazolin-2-one and 2-amino-6-(2-thienyl)purine in replication and transcription.
2002
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:40:59 GMT 2025
Edited
by admin
on Mon Mar 31 18:40:59 GMT 2025
Record UNII
2K48456N55
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYLENEUREA
HSDB  
Preferred Name English
IMIDAZOLIDINONE
INCI  
INCI  
Official Name English
2-IMIDAZOLINONE
Systematic Name English
NSC-21314
Code English
2-IMIDAZOLIDINONE
MI  
Systematic Name English
1,3-ETHYLENEUREA
Common Name English
ETHYLENE UREA
Systematic Name English
2-IMIDAZOLIDINONE [MI]
Common Name English
ETHYLENEUREA [HSDB]
Common Name English
Code System Code Type Description
NSC
21314
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID0020602
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
MESH
C004916
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
HSDB
4021
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
CAS
120-93-4
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
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MERCK INDEX
m6225
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY Merck Index
CHEBI
37001
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
RXCUI
2565925
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-436-4
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
FDA UNII
2K48456N55
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY
PUBCHEM
8453
Created by admin on Mon Mar 31 18:40:59 GMT 2025 , Edited by admin on Mon Mar 31 18:40:59 GMT 2025
PRIMARY