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Molecule
ID:75641
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₄BrNO₂S
Molecular Mass
304.20336
Exact Mass
302.99286169
Charge
0
InChI
InChI=1S/C11H14BrNO2S/c12-10-6-2-3-7-11(10)16(14,15)13-8-4-1-5-9-13/h2-3,6-7H,1,4-5,8-9H2
InChIKey
QVJWVAUVIDEPPD-UHFFFAOYSA-N
Canonic Smiles
Brc1ccccc1S(=O)(=O)N1CCCCC1
Isomeric Smiles
S(=O)(=O)(N1CCCCC1)c1ccccc1Br
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
2.6457474
LogD (pH = 7.4)
2.6457474
Log P
2.6457474
Molar Refractivity
67.7741
Polarizability
26.929956
Polar Surface Area
37.38
Rotatable Bonds
1
Lipinski's Rule of Five
true
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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
Names and Identifiers
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IUPAC name
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IUPAC Traditional name
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Synonyms
Registration numbers
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
Properties
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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
Apollo Scientific
OR11632
Alfa Aesar
H60748
Academic Data
PubChem
26370022
Names and Identifiers
IUPAC name
1-(2-bromobenzenesulfonyl)piperidine
IUPAC Traditional name
1-(2-bromobenzenesulfonyl)piperidine
Synonyms
1-[(2-Bromophenyl)sulphonyl]piperidine
1-(2-Bromophenylsulfonyl)piperidine
Registration numbers
MDL Number
MFCD09800969
CAS Number
951883-98-0
PubChem CID
26370022
PubChem SID
162040559
Properties
Safety Information
Storage Warning
Irritant
Source
Risk Statements
36/37/38
Source
Safety Statements
26
-
37
-
60
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 Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-
P501
Source
European Hazard Symbols
Irritant (Xi)
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
TSCA Listed
否
Source
Product Information
Purity
97%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay