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Molecule
ID:8922
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₉BrO₂
Molecular Mass
229.07056
Exact Mass
227.97859153
Charge
0
InChI
InChI=1S/C9H9BrO2/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-4H,5-6H2,(H,11,12)
InChIKey
AOACQJFIGWNQBC-UHFFFAOYSA-N
Canonic Smiles
OC(=O)CCc1ccccc1Br
Isomeric Smiles
O=C(CCc1ccccc1Br)O
Calculated Properties
JChem
Acid pKa
3.413179
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.749349
LogD (pH = 7.4)
-0.5752313
Log P
2.8243153
Molar Refractivity
49.5894
Polarizability
19.225086
Polar Surface Area
37.3
Rotatable Bonds
3
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
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
•
RDKit
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JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC name
•
IUPAC Traditional name
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Synonyms
Registration numbers
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR3083
Matrix Scientific
004939
Sigma Aldrich
643912
Enamine
EN300-42626
Bide Pharmatech
BD7664
Alfa Aesar
H33933
A&J Pharmtech
AJA-O40461
Academic Data
PubChem
316010
Names and Identifiers
IUPAC name
3-(2-bromophenyl)propanoic acid
IUPAC Traditional name
3-(2-bromophenyl)propanoic acid
Synonyms
3-(2-Bromophenyl)propionic acid
3-(2-Bromophenyl)propanoic acid
3-(2-Bromophenyl)propionic acid
3-(2-溴苯基)丙酸
Registration numbers
CAS Number
15115-58-9
MDL Number
MFCD01310791
PubChem SID
24883301
160972229
PubChem CID
316010
Molecule Details
Sigma Aldrich
643912
Packaging
5, 25 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
96-98°C
Source
98-102 °C(lit.)
Source
95 - 97°C
Source
93-95°C
Source
Hydrophobicity(logP)
2.766
Source
Safety Information
TSCA Listed
false
Source
否
Source
Download link
Source
Download link
Source
IRRITANT
Source
Irritant
Source
Harmful (Xn)
2
Source
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
P261
-
P305+P351+P338
Source
P261
-
P301+P310
-
P305+P351+P338
-
P302+P352
-
P405
-P501A
Source
26
-
36
Source
26
-
36/37
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
Warning
Source
H302
-
H315
-
H319
-
H335
Source
H301
-
H315
-
H319
-
H335
Source
22
-
36/37/38
Source
Product Information
98%
Source
97%
Source
95%
Source
96%
Source
C9H9BrO2
Source
Source
Harmful (X)
Source
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
MSDS Link
Storage Warning
European Hazard Symbols
German water hazard class
GHS Pictograms
GHS Precautionary statements
Safety Statements
Personal Protective Equipment
GHS Signal Word
GHS Hazard statements
Risk Statements
Purity
Empirical Formula (Hill Notation)