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Molecule
ID:65066
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₅BO₂Si
Molecular Mass
194.1107
Exact Mass
194.09343665
Charge
0
InChI
InChI=1S/C9H15BO2Si/c1-13(2,3)9-6-4-8(5-7-9)10(11)12/h4-7,11-12H,1-3H3
InChIKey
NRPZMSUGPMYBCQ-UHFFFAOYSA-N
Canonic Smiles
OB(c1ccc(cc1)[Si](C)(C)C)O
Isomeric Smiles
B(c1ccc([Si](C)(C)C)cc1)(O)O
Calculated Properties
JChem
Acid pKa
8.760488
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
3.224163
LogD (pH = 7.4)
3.205964
Log P
3.2244
Molar Refractivity
46.6671
Polarizability
21.991592
Polar Surface Area
40.46
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
1710
Commercial Catalog
Sigma Aldrich
523674
Matrix Scientific
070397
Bide Pharmatech
BD7031
A&J Pharmtech
AJA-O39000
Names and Identifiers
Synonyms
4-Trimethylsilylphenylboronic acid
4-(Trimethylsilyl)phenylboronic acid
4-(三甲基硅烷)苯硼酸
(4-(Trimethylsilyl)phenyl)boronic acid
IUPAC name
[4-(trimethylsilyl)phenyl]boronic acid
IUPAC Traditional name
4-(trimethylsilyl)phenylboronic acid
Registration numbers
MDL Number
MFCD00093348
CAS Number
17865-11-1
PubChem CID
1710
PubChem SID
162030805
24874358
Molecule Details
Sigma Aldrich
523674
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
97+%
Source
≥95.0%
Source
97%
Source
98%
Source
Linear Formula
(CH3)3SiC6H4B(OH)2
Source
Safety Information
MSDS Link
Download link
Source
Download link
Source
false
Source
IRRITANT
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Physical Property
173-178 °C(lit.)
Source
TSCA Listed
Storage Warning
German water hazard class
Personal Protective Equipment
Melting Point