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Molecule
ID:102728
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₈O₇
Molecular Mass
286.27782
Exact Mass
286.10525292
Charge
0
InChI
InChI=1S/C13H18O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-4,9-18H,5-6H2
InChIKey
NGFMICBWJRZIBI-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(Oc2ccccc2CO)C(C(C1O)O)O
Isomeric Smiles
OCC1OC(Oc2c(CO)cccc2)C(O)C(O)C1O
Calculated Properties
JChem
Acid pKa
12.19871
H Acceptors
7
H Donor
5
LogD (pH = 5.5)
-1.3657374
LogD (pH = 7.4)
-1.3657442
Log P
-1.3657373
Molar Refractivity
66.9992
Polarizability
27.106068
Polar Surface Area
119.61
Rotatable Bonds
4
Lipinski's Rule of Five
true
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MP Biomedicals
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Data Source
Commercial Catalog
MP Biomedicals
02102833
Academic Data
PubChem
5145
Names and Identifiers
IUPAC Traditional name
salicin
IUPAC name
2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol
Synonyms
SALICIN
Salicoside
2-(Hydroxymethyl)phenyl-β-D-glucopyranoside
Registration numbers
CAS Number
138-52-3
EC Number
205-331-6
PubChem SID
162090665
PubChem CID
5145
Properties
Product Information
Certificate of Analysis
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Source
Physical Property
Melting Point
197-200°C
Source
Safety Information
RTECS
LZ5901700
Source
Storage Condition
Room Temperature (15-30°C)
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MSDS Link
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Molecule Details
MP Biomedicals
02102833
Crystalline
Substrate for β-glucosidase.
References
PubChem Literature
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Bioactivity
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