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Molecule
ID:43418
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₀BrNO₂
Molecular Mass
268.1066
Exact Mass
266.98949057
Charge
0
InChI
InChI=1S/C11H10BrNO2/c1-2-15-11(14)10-5-7-3-4-8(12)6-9(7)13-10/h3-6,13H,2H2,1H3
InChIKey
FVMZWWFKRMBNSZ-UHFFFAOYSA-N
Canonic Smiles
CCOC(=O)c1cc2c([nH]1)cc(cc2)Br
Isomeric Smiles
c1([nH]c2c(c1)ccc(c2)Br)C(=O)OCC
Calculated Properties
JChem
Acid pKa
10.982136
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
3.121045
LogD (pH = 7.4)
3.1209466
Log P
3.1210465
Molar Refractivity
61.4187
Polarizability
24.540771
Polar Surface Area
42.09
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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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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From Data Sources
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
046758
Apollo Scientific
OR41055
Key Organics
DC-0707
Enamine
EN300-60688
Bide Pharmatech
BD17365
Academic Data
PubChem
7009496
Names and Identifiers
IUPAC name
ethyl 6-bromo-1H-indole-2-carboxylate
IUPAC Traditional name
ethyl 6-bromo-1H-indole-2-carboxylate
Synonyms
Ethyl 6-bromo-1H-indole-2-carboxylate
6-Bromo-2-(ethoxylcarbonyl)-1H-indole
Ethyl 6-bromoindole-2-carboxylate
Registration numbers
CAS Number
103858-53-3
MDL Number
MFCD03094942
PubChem CID
7009496
PubChem SID
162048181
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
Harmful/Irritant
Source
MSDS Link
Download link
Source
TSCA Listed
false
Source
Product Information
Purity
>95%
Source
95%
Source
95+%
Source
Physical Property
187 - 189°C
Source
3.96
Source
Melting Point
Hydrophobicity(logP)