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Molecule
ID:14685
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₁NO₄
Molecular Mass
221.20934
Exact Mass
221.06880784
Charge
0
InChI
InChI=1S/C11H11NO4/c1-15-8-3-4-9(16-2)10-6(8)5-7(12-10)11(13)14/h3-5,12H,1-2H3,(H,13,14)
InChIKey
FJWNGDWJFIQNEG-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(c2c1[nH]c(c2)C(=O)O)OC
Isomeric Smiles
c12c(c(ccc1OC)OC)[nH]c(c2)C(=O)O
Calculated Properties
JChem
Acid pKa
3.654857
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-0.5081609
LogD (pH = 7.4)
-1.988839
Log P
1.3342493
Molar Refractivity
57.2046
Polarizability
22.91675
Polar Surface Area
71.55
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
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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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JChem
Data Source
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC name
Registration numbers
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CAS Number
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MDL Number
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PubChem CID
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PubChem SID
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
012221
InterBioScreen
BB_NC-0878
STOCK1N-38082
Enamine
EN300-15091
Academic Data
PubChem
510118
Names and Identifiers
IUPAC Traditional name
4,7-dimethoxy-1H-indole-2-carboxylic acid
Synonyms
4,7-Dimethoxy-1H-indole-2-carboxylic acid
IUPAC name
4,7-dimethoxy-1H-indole-2-carboxylic acid
Registration numbers
CAS Number
31271-83-7
MDL Number
MFCD02664474
PubChem CID
510118
PubChem SID
160977992
Properties
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Product Information
Classification
Derivatives & analogs of Natural Compounds
Source
Purity
95%
Source
Physical Property
Hydrophobicity(logP)
2.087
Source
Melting Point
201 - 203°C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay