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5-Isopropyl-2-methoxyphenylboronic acid_Molecular_structure_CAS_216393-63-4)
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5-Isopropyl-2-methoxyphenylboronic acid

Catalog No. 680583 Name Sigma Aldrich
CAS Number 216393-63-4 Website http://www.sigmaaldrich.com
M. F. C10H15BO3 Telephone 1-800-521-8956
M. W. 194.0353 Fax
Purity Email
Storage Chembase ID: 140785

SYNONYMS

Title
5-异丙基-2-甲氧基苯硼酸
IUPAC name
[2-methoxy-5-(propan-2-yl)phenyl]boronic acid
IUPAC Traditional name
5-isopropyl-2-methoxyphenylboronic acid
Synonyms
[2-Methoxy-5-(1-methylethyl)phenyl]boronic acid
5-Isopropyl-2-methoxybenzeneboronic acid

DATABASE IDS

CAS Number 216393-63-4
PubChem SID 24885577
MDL Number MFCD01318154

PROPERTIES

Empirical Formula (Hill Notation) C10H15BO3
Melting Point 84-88 °C
MSDS Link Download
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
General description
May contain varying amounts of anhydride
Packaging
1, 10 g in glass bottle
Application
Reactant involved in the synthesis of many biologically active molecules including:
• Oxazolidinones for use as cholesteryl ester transfer protein inhibitors for atherosclerosis treatment1,2
• Selective quinazolinyl-phenol inhibitors of CHK1 as antitumor and radioprotectants3
• Biaryl-containing carbamates as CETP inhibitors4
• α -Sulfone hydroxamates as MMP inhibitors5Reactant involved in Suzuki-Miyaura cross coupling with 2-nitroarenediazonium tetrafluoroborate for synthesis of 2-nitrobiphenyls6
Description (简体中文)
General description
可能含不定量的酸酐
包装
1, 10 g in glass bottle
Application
Reactant involved in the synthesis of many biologically active molecules including:
• Oxazolidinones for use as cholesteryl ester transfer protein inhibitors for atherosclerosis treatment1,2
• Selective quinazolinyl-phenol inhibitors of CHK1 as antitumor and radioprotectants3
• Biaryl-containing carbamates as CETP inhibitors4
• α -Sulfone hydroxamates as MMP inhibitors5Reactant involved in Suzuki-Miyaura cross coupling with 2-nitroarenediazonium tetrafluoroborate for synthesis of 2-nitrobiphenyls6

REFERENCES