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Molecule
ID:75638
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₄BrNO
Molecular Mass
256.13896
Exact Mass
255.02587607
Charge
0
InChI
InChI=1S/C11H14BrNO/c1-8(2)7-13-11(14)9-3-5-10(12)6-4-9/h3-6,8H,7H2,1-2H3,(H,13,14)
InChIKey
JAHXIBMUKXWKFH-UHFFFAOYSA-N
Canonic Smiles
CC(CNC(=O)c1ccc(cc1)Br)C
Isomeric Smiles
N(CC(C)C)C(=O)c1ccc(cc1)Br
Calculated Properties
JChem
Acid pKa
14.790332
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
3.0606177
LogD (pH = 7.4)
3.060618
Log P
3.060618
Molar Refractivity
61.4001
Polarizability
23.295383
Polar Surface Area
29.1
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Related Proteins
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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
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RDKit
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IUPAC Traditional name
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IUPAC name
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Synonyms
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
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Product Information
Related Proteins
Molecular Spectra
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR11628
Alfa Aesar
H57385
Academic Data
PubChem
698466
Names and Identifiers
IUPAC Traditional name
4-bromo-N-(2-methylpropyl)benzamide
IUPAC name
4-bromo-N-(2-methylpropyl)benzamide
Synonyms
4-Bromo-N-isobutylbenzamide
4-Bromo-N-isobutylbenzamide
Registration numbers
MDL Number
MFCD01212030
CAS Number
161768-66-7
PubChem CID
698466
PubChem SID
162040556
Properties
Safety Information
Storage Warning
Irritant
Source
Risk Statements
36/37/38
Source
GHS Precautionary statements
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-
P501
Source
GHS Hazard statements
H315
-
H319
-
H335
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
European Hazard Symbols
Irritant (Xi)
Source
Product Information
Purity
97%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay