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Molecule
ID:33192
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₇BrO₂
Molecular Mass
215.04398
Exact Mass
213.96294146
Charge
0
InChI
InChI=1S/C8H7BrO2/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4H,5H2,(H,10,11)
InChIKey
FTPAHNNMUYOHOB-UHFFFAOYSA-N
Canonic Smiles
BrCc1cccc(c1)C(=O)O
Isomeric Smiles
C(=O)(c1cc(CBr)ccc1)O
Calculated Properties
JChem
Acid pKa
4.035023
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.9276793
LogD (pH = 7.4)
-0.73507196
Log P
2.4035661
Molar Refractivity
46.1646
Polarizability
17.304707
Polar Surface Area
37.3
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Properties
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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
Calculated Properties
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RDKit
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IUPAC Traditional name
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IUPAC name
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MDL Number
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
035938
TRC
B685280
Enamine
EN300-11618
Bide Pharmatech
BD40796
Academic Data
PubChem
245650
Names and Identifiers
Synonyms
3-(Bromomethyl)benzoic acid
m-Bromomethylbenzoic Acid
NSC 57780
α-Bromo-m-toluic Acid
3-Carboxybenzyl Bromide
IUPAC Traditional name
3-(bromomethyl)benzoic acid
IUPAC name
3-(bromomethyl)benzoic acid
Registration numbers
PubChem SID
160996499
PubChem CID
245650
CAS Number
6515-58-8
MDL Number
MFCD00045839
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
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Source
TSCA Listed
false
Source
Product Information
Certificate of Analysis
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Source
95%
Source
85%
Source
Physical Property
DMSO
Source
Methanol
Source
Off-White Solid
Source
136-140°C
Source
115 - 130°C
Source
2.667
Source
Purity
Solubility
Apperance
Melting Point
Hydrophobicity(logP)