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Molecule
ID:32877
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₃BO₃
Molecular Mass
180.00872
Exact Mass
180.09577468
Charge
0
InChI
InChI=1S/C9H13BO3/c1-7(2)13-9-5-3-8(4-6-9)10(11)12/h3-7,11-12H,1-2H3
InChIKey
CJUHQADBFQRIMC-UHFFFAOYSA-N
Canonic Smiles
OB(c1ccc(cc1)OC(C)C)O
Isomeric Smiles
c1(ccc(cc1)OC(C)C)B(O)O
Calculated Properties
JChem
Acid pKa
8.877205
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
2.1425188
LogD (pH = 7.4)
2.1285388
Log P
2.1427
Molar Refractivity
46.2341
Polarizability
19.731148
Polar Surface Area
49.69
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Properties
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Related Proteins
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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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From Data Sources
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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4009733
Matrix Scientific
035611
Apollo Scientific
OR14157
Sigma Aldrich
542474
Bide Pharmatech
BD6939
A&J Pharmtech
AJA-O34971
Academic Data
PubChem
3698726
Names and Identifiers
Synonyms
4-Isopropoxylphenylboronic acid
(4-isopropoxyphenyl)boronic acid
4-Isopropoxybenzeneboronic acid
1-Borono-4-isopropoxybenzene
4-Isopropoxyphenylboronic acid
4-Isopropoxybenzeneboronic acid
4-异丙氧基苯硼酸
4-(1-Methylethoxy)phenylboronic acid
4-Isopropyloxyphenylboronic acid
4-Isopropoxyphenylboronic acid
IUPAC name
[4-(propan-2-yloxy)phenyl]boronic acid
IUPAC Traditional name
4-isopropoxyphenylboronic acid
Registration numbers
MDL Number
MFCD03427051
CAS Number
153624-46-5
PubChem SID
24878606
160996184
PubChem CID
3698726
Molecule Details
Sigma Aldrich
542474
General description
Contains varying amounts of anhydride
Packaging
1, 10 g in glass bottle
Application
Reactant for:
• Microwave-mediated click-chemistry synthesis of glyco-porphyrin derivatives with in vitro photo-cytotoxicity for application in photodynamic therapy1
• Palladium-catalyzed oxidative cross-coupling reactions2
• Ruthenium-catalyzed hydrogenation reactions3
• Stereoselective rhodium-catalyzed arylation4
• Palladium acetate catalyzed C-glycosidation5
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Irritant
Source
MSDS Link
Download link
Source
Download link
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
3
Source
Product Information
98%
Source
C6H4OCH(CH3)2B(OH)2
Source
Personal Protective Equipment
German water hazard class
Purity
Linear Formula