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Molecule
ID:109278
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₆N₄O₂
Molecular Mass
142.11604
Exact Mass
142.04907545
Charge
0
InChI
InChI=1S/C4H6N4O2/c9-3-5-1-2(7-3)8-4(10)6-1/h1-2H,(H2,5,7,9)(H2,6,8,10)
InChIKey
VPVSTMAPERLKKM-UHFFFAOYSA-N
Canonic Smiles
O=C1NC2C(N1)NC(=O)N2
Isomeric Smiles
O=C1NC2NC(=O)NC2N1
Calculated Properties
JChem
LogD (pH = 7.4)
-1.70
LogD (pH = 5.5)
-1.70
Log P
-1.70
Rotatable Bonds
0
H Donor
4
H Acceptors
2
Lipinski's Rule of Five
true
Acid pKa
11.69
Polar Surface Area
82.26
Polarizability
11.82
Molar Refractivity
29.44
LOG S
0.08
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Academic Data
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Commercial Catalog
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
Properties
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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MP Biomedicals
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
62347
ChEBI
CHEBI:42946
Commercial Catalog
Sigma Aldrich
G7305
MP Biomedicals
05210437
Bide Pharmatech
BD41725
Names and Identifiers
IUPAC name
octahydroimidazo[4,5-d]imidazolidine-2,5-dione
octahydro-[1,3]diazolo[4,5-d]imidazole-2,5-dione
Synonyms
ACETYLENE DIUREIN
NSC 2765
Acetylenediurea
Glycoluril
乙炔脲
Acetylene carbamide
甘脲
Tetrahydroimidazo[4,5-d]imidazole-2,5-dione
Tetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione
acetylenediureine
acetyleneurea
glycoluril
acetylene carbamide
glyoxalbiuret
glyoxaldiureine
diurea glyoxalate
glycoluril
IUPAC Traditional name
acetylenediureine
glycoluril
Registration numbers
CAS Number
496-46-8
PubChem SID
162094954
24895300
26697231
PubChem CID
62347
Beilstein Number
128826
MDL Number
MFCD00005539
EC Number
207-821-5
Patent number
WO2005103053
EP0856563
US2005080068
WO2005087777
WO2007106144
CHEMBL
CHEMBL3182837
DrugBank ID
DB03533
SureChEMBL Database
SCHEMBL36249
CompTox Database
DTXSID6031380
CHEBI ID
CHEBI:37082
CHEBI:42940
CHEBI:42946
ACToR Database
496-46-8
Properties
Product Information
Certificate of Analysis
Download link
Source
Purity
97%
Source
95+%
Source
Empirical Formula (Hill Notation)
C4H6N4O2
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
GHS Signal Word
Warning
Source
German water hazard class
1
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
GHS Hazard statements
H302
Source
Risk Statements
22
Source
European Hazard Symbols
Harmful (Xn)
Source
Physical Property
Melting Point
>300 °C(lit.)
Source
Molecule Details
Sigma Aldrich
G7305
Packaging
100 g in poly bottle
5 g in glass bottle
Application
Reactant involved in synthesis of:
• Glycouril hexamers and monofunctionalized cucurbit[6]uril derivatives1,2,3
• N-chloro compounds from trichloroisocyanuric acid4
• Glycouril trimers5
MP Biomedicals
05210437
MP Biomedicals Rare Chemical collection
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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PubChem SID
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PubChem CID
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Beilstein Number
•
MDL Number
•
EC Number
•
Patent number
•
CHEMBL
•
DrugBank ID
•
SureChEMBL Database
•
CompTox Database
•
CHEBI ID
•
ACToR Database