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Molecule
ID:131506
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₃₂O₃Si₃
Molecular Mass
308.63718
Exact Mass
308.16592448
Charge
0
InChI
InChI=1S/C12H32O3Si3/c1-16(2,3)13-10-12(15-18(7,8)9)11-14-17(4,5)6/h12H,10-11H2,1-9H3
InChIKey
JQUGYGVCECHKBA-UHFFFAOYSA-N
Canonic Smiles
C[Si](OC(CO[Si](C)(C)C)CO[Si](C)(C)C)(C)C
Isomeric Smiles
C[Si](C)(C)OCC(CO[Si](C)(C)C)O[Si](C)(C)C
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
4.425
LogD (pH = 7.4)
4.425
Log P
4.425
Molar Refractivity
68.8938
Polarizability
33.71874
Polar Surface Area
27.69
Rotatable Bonds
8
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
No Data Available
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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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Commercial Catalog
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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 SID
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PubChem CID
Properties
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Safety 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
Sigma Aldrich
T1017
Academic Data
PubChem
522285
Names and Identifiers
IUPAC Traditional name
2,2,8,8-tetramethyl-5-[(trimethylsilyl)oxy]-3,7-dioxa-2,8-disilanonane
Synonyms
Trimethylsilylglycerol
IUPAC name
2,2,8,8-tetramethyl-5-[(trimethylsilyl)oxy]-3,7-dioxa-2,8-disilanonane
Registration numbers
CAS Number
6787-10-6
MDL Number
MFCD00171728
PubChem SID
162225784
PubChem CID
522285
Properties
Safety Information
Storage Temperature
2-8°C
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Physical Property
Apperance
clear, colorless
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay