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Molecule
ID:48403
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₀ClN₃O
Molecular Mass
199.6375
Exact Mass
199.05123964
Charge
0
InChI
InChI=1S/C8H10ClN3O/c9-7-3-10-4-8(11-7)12-2-1-6(13)5-12/h3-4,6,13H,1-2,5H2
InChIKey
XEFKCMOGRCBXAO-UHFFFAOYSA-N
Canonic Smiles
OC1CCN(C1)c1cncc(n1)Cl
Isomeric Smiles
N1(c2nc(Cl)cnc2)CC(CC1)O
Calculated Properties
JChem
Acid pKa
14.829832
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
0.32272184
LogD (pH = 7.4)
0.322724
Log P
0.32272404
Molar Refractivity
51.2113
Polarizability
18.95481
Polar Surface Area
49.25
Rotatable Bonds
1
Lipinski's Rule of Five
true
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
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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
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Academic Data
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Synonyms
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IUPAC Traditional name
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IUPAC name
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PubChem SID
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PubChem CID
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MDL Number
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
051891
Enamine
EN300-80221
A&J Pharmtech
AJA-O21024
Academic Data
PubChem
53408184
Names and Identifiers
Synonyms
1-(6-Chloro-2-pyrazinyl)-3-pyrrolidinol
1-(6-chloropyrazin-2-yl)pyrrolidin-3-ol
IUPAC Traditional name
1-(6-chloropyrazin-2-yl)pyrrolidin-3-ol
IUPAC name
1-(6-chloropyrazin-2-yl)pyrrolidin-3-ol
Registration numbers
PubChem SID
162053166
PubChem CID
53408184
MDL Number
MFCD09879058
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Product Information
Purity
95%
Source
98%
Source
Physical Property
0.121
Source
80 - 82°C
Source
Hydrophobicity(logP)
Melting Point