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Molecule
ID:104019
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₆O₇
Molecular Mass
284.26194
Exact Mass
284.08960285
Charge
0
InChI
InChI=1S/C13H16O7/c14-5-7-1-3-8(4-2-7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-5,9-13,15-18H,6H2
InChIKey
OLZAGZCCJJBKNZ-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(Oc2ccc(cc2)C=O)C(C(C1O)O)O
Isomeric Smiles
OCC1OC(Oc2ccc(C=O)cc2)C(O)C(O)C1O
Calculated Properties
JChem
Acid pKa
12.200142
H Acceptors
7
H Donor
4
LogD (pH = 5.5)
-0.88588536
LogD (pH = 7.4)
-0.88589215
Log P
-0.88588524
Molar Refractivity
66.7673
Polarizability
26.55684
Polar Surface Area
116.45
Rotatable Bonds
4
Lipinski's Rule of Five
true
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MP Biomedicals
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02153983
InterBioScreen
STOCK1N-75824
Academic Data
PubChem
3303383
Names and Identifiers
Synonyms
HELICID
Salicylaldehyde β-D-glucoside
p-Benzaldehydyl-β-D-Allopyranoside
IUPAC Traditional name
4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde
IUPAC name
4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}benzaldehyde
Registration numbers
EC Number
210-558-9
CAS Number
618-65-5
PubChem CID
3303383
PubChem SID
162090919
Properties
Product Information
Certificate of Analysis
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Source
Purity
~99%
Source
Classification
Genuine Natural Compounds
Source
Safety Information
MSDS Link
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Source
Storage Condition
Room Temperature (15-30°C)
Source
Molecule Details
MP Biomedicals
02153983
Plant source: Helicia erralica
Purity: ~99%
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay