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4-Isopropoxyphenylboronic acid_Molecular_structure_CAS_153624-46-5)
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4-Isopropoxyphenylboronic acid

Catalog No. 542474 Name Sigma Aldrich
CAS Number 153624-46-5 Website http://www.sigmaaldrich.com
M. F. C9H13BO3 Telephone 1-800-521-8956
M. W. 180.00872 Fax
Purity Email
Storage Chembase ID: 32877

SYNONYMS

Title
4-异丙氧基苯硼酸
IUPAC name
[4-(propan-2-yloxy)phenyl]boronic acid
IUPAC Traditional name
4-isopropoxyphenylboronic acid
Synonyms
4-Isopropoxybenzeneboronic acid
4-(1-Methylethoxy)phenylboronic acid
4-Isopropyloxyphenylboronic acid

DATABASE IDS

CAS Number 153624-46-5
PubChem SID 24878606
MDL Number MFCD03427051

PROPERTIES

German water hazard class 3
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Linear Formula C6H4OCH(CH3)2B(OH)2

DETAILS

Description (English)
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
Description (简体中文)
General description
含不定量的酸酐
包装
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