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Molecule
ID:50899
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₁₅ClN₂O₂S
Molecular Mass
214.7135
Exact Mass
214.05427641
Charge
0
InChI
InChI=1S/C6H14N2O2S.ClH/c1-11(9,10)8-4-2-6(7)3-5-8;/h6H,2-5,7H2,1H3;1H
InChIKey
BASBDQBWDDKEDK-UHFFFAOYSA-N
Canonic Smiles
NC1CCN(CC1)S(=O)(=O)C.Cl
Isomeric Smiles
S(=O)(=O)(N1CCC(CC1)N)C.Cl
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-4.894478
LogD (pH = 7.4)
-4.324154
Log P
-1.8767196
Molar Refractivity
43.2421
Polarizability
17.934917
Polar Surface Area
63.4
Rotatable Bonds
0
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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Quote
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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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IUPAC Traditional name
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IUPAC name
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CAS Number
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PubChem CID
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MDL Number
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PubChem SID
Properties
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Safety Information
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Physical Property
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Product Information
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
054427
Enamine
EN300-26205
Bide Pharmatech
BD51748
A&J Pharmtech
AJA-O10717
Academic Data
PubChem
17221636
Names and Identifiers
Synonyms
1-Methanesulfonyl-piperidin-4-ylamine hydrochloride
1-(methylsulfonyl)piperidin-4-amine hydrochloride
IUPAC Traditional name
1-methanesulfonylpiperidin-4-amine hydrochloride
IUPAC name
1-methanesulfonylpiperidin-4-amine hydrochloride
Registration numbers
CAS Number
651057-01-1
PubChem CID
17221636
MDL Number
MFCD08690153
PubChem SID
162055662
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
Physical Property
Hydrophobicity(logP)
-1.406
Source
Melting Point
269 - 271°C
Source
Product Information
95%
Source
95+%
Source
97%
Source
HCl
Source
Purity
Salt Data