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
SMILES
O=C1NCCN1
InChI
InChIKey=YAMHXTCMCPHKLN-UHFFFAOYSA-N
InChI=1S/C3H6N2O/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)
| 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
| Title | Date | PubMed |
|---|---|---|
| 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 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:40:59 GMT 2025
by
admin
on
Mon Mar 31 18:40:59 GMT 2025
|
| Record UNII |
2K48456N55
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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
|
PRIMARY | |||
|
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 | ||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 | |||
|
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 |