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Molecule
ID:44351
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₂BrNO₂
Molecular Mass
282.13318
Exact Mass
281.00514063
Charge
0
InChI
InChI=1S/C12H12BrNO2/c1-3-16-12(15)11-7-8-6-9(13)4-5-10(8)14(11)2/h4-7H,3H2,1-2H3
InChIKey
RLEUBLNVHZTFOH-UHFFFAOYSA-N
Canonic Smiles
CCOC(=O)c1cc2c(n1C)ccc(c2)Br
Isomeric Smiles
c1(n(c2c(c1)cc(cc2)Br)C)C(=O)OCC
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
3.3447225
LogD (pH = 7.4)
3.3447225
Log P
3.3447225
Molar Refractivity
66.3154
Polarizability
26.29015
Polar Surface Area
31.23
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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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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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR14054
Key Organics
KA-0922
Matrix Scientific
047781
Academic Data
PubChem
11637730
Names and Identifiers
IUPAC Traditional name
ethyl 5-bromo-1-methylindole-2-carboxylate
Synonyms
Ethyl 5-bromo-1-methyl-1H-indole-2-carboxylate
IUPAC name
ethyl 5-bromo-1-methyl-1H-indole-2-carboxylate
Registration numbers
MDL Number
MFCD09027165
CAS Number
91844-20-1
91844-20-1
PubChem CID
11637730
PubChem SID
162049114
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
Product Information
Purity
>95%
Source
Physical Property
Melting Point
83-85°C
Source
83 - 85 °C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay