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Molecule
ID:131305
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₈H₁₆SSi
Molecular Mass
292.47014
Exact Mass
292.07419804
Charge
0
InChI
InChI=1S/C18H16SSi/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19H
InChIKey
MQDRKELSDPESDZ-UHFFFAOYSA-N
Canonic Smiles
S[Si](c1ccccc1)(c1ccccc1)c1ccccc1
Isomeric Smiles
c1ccc(cc1)[Si](c1ccccc1)(c1ccccc1)S
Calculated Properties
JChem
Acid pKa
10.171324
H Acceptors
0
H Donor
1
LogD (pH = 5.5)
5.6743913
LogD (pH = 7.4)
5.673693
Log P
5.6744
Molar Refractivity
82.9787
Polarizability
35.605717
Polar Surface Area
0.0
Rotatable Bonds
3
Lipinski's Rule of Five
false
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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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
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
T6925
422150
93132
Academic Data
PubChem
621128
Names and Identifiers
Synonyms
Mercaptotriphenylsilane
三苯基硅烷硫醇
Triphenylsilanethiol
IUPAC name
triphenylsilanethiol
IUPAC Traditional name
triphenylsilanethiol
Registration numbers
CAS Number
14606-42-9
PubChem SID
24866296
24889804
162225583
MDL Number
MFCD00192551
Beilstein Number
2941369
PubChem CID
621128
Molecule Details
Sigma Aldrich
422150
Packaging
5 g in glass bottle
93132
Other Notes
Solid equivalent of H2S. Opening of epoxides to β-hydroxy thiols1; Free-radical addition to olefins to give thiols2
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
PubChem SID
•
MDL Number
•
Beilstein Number
•
PubChem CID
Properties
Physical Property
Melting Point
101-104 °C(lit.)
Source
101-104 °C
Source
Safety Information
Storage Temperature
2-8°C
Source
Safety Statements
22
-
24/25
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Download link
Source
Download link
Source
Product Information
(C6H5)3SiSH
Source
98%
Source
≥97.0% (GC)
Source
purum
Source
German water hazard class
Personal Protective Equipment
MSDS Link
Linear Formula
Purity
Grade