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Molecule
ID:121617
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₇BrO₃
Molecular Mass
267.07548
Exact Mass
265.95785608
Charge
0
InChI
InChI=1S/C11H7BrO3/c12-8-3-1-7(2-4-8)9-5-6-10(15-9)11(13)14/h1-6H,(H,13,14)
InChIKey
MYPDSPQSFHXXTF-UHFFFAOYSA-N
Canonic Smiles
Brc1ccc(cc1)c1ccc(o1)C(=O)O
Isomeric Smiles
o1c(ccc1c1ccc(cc1)Br)C(=O)O
Calculated Properties
JChem
Acid pKa
3.1394627
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.6931076
LogD (pH = 7.4)
-0.4284436
Log P
3.0270545
Molar Refractivity
58.3416
Polarizability
23.279055
Polar Surface Area
50.44
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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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
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IUPAC Traditional name
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IUPAC name
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PubChem CID
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MDL Number
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_SC-1985
Sigma Aldrich
568295
Academic Data
PubChem
741099
Names and Identifiers
Synonyms
5-(4-bromophenyl)furan-2-carboxylic acid
5-(4-溴苯基)-2-糠酸
5-(4-Bromophenyl)-2-furoic acid
IUPAC Traditional name
5-(4-bromophenyl)furan-2-carboxylic acid
IUPAC name
5-(4-bromophenyl)furan-2-carboxylic acid
Registration numbers
PubChem SID
162215970
24880435
PubChem CID
741099
CAS Number
52938-96-2
MDL Number
MFCD00194276
Molecule Details
Sigma Aldrich
568295
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
205-209 °C(lit.)
Source
Product Information
Purity
98%
Source
Empirical Formula (Hill Notation)
C11H7BrO3
Source
Safety Information
German water hazard class
3
Source
MSDS Link
Download link
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Personal Protective Equipment