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4-Methoxy-2-methylphenylboronic acid_Molecular_structure_CAS_208399-66-0)
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4-Methoxy-2-methylphenylboronic acid

Catalog No. 639370 Name Sigma Aldrich
CAS Number 208399-66-0 Website http://www.sigmaaldrich.com
M. F. C8H11BO3 Telephone 1-800-521-8956
M. W. 165.98214 Fax
Purity Email
Storage Chembase ID: 32756

SYNONYMS

Title
4-甲氧基-2-甲基苯硼酸
IUPAC name
(4-methoxy-2-methylphenyl)boronic acid
IUPAC Traditional name
4-methoxy-2-methylphenylboronic acid
Synonyms
2-Methyl-4-methoxybenzeneboronic acid
4-Methoxy-2-methylbenzeneboronic acid
2-Methyl-4-methoxyphenylboronic acid

DATABASE IDS

CAS Number 208399-66-0
MDL Number MFCD02684315
PubChem SID 24883021

PROPERTIES

Linear Formula CH3OC6H3(CH3)B(OH)2
Melting Point 169-174 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant for preparation of biologically active molecules:
• Preparation of hydroxyphenylnaphthols as 17β-hydroxysteroid dehydrogenase Type 2 inhibitors1Reactant for:
• Preparation of axially-chiral biarylphosphonates by asymmetric Suzuki coupling catalyzed by palladium complexes with helically-chiral polyquinoxaline phosphine and polyphosphine copolymers2
• Preparation of arylpyrimidines and their use in regioselective acetoxylation3
• Preparation of N-arylated azoles via copper fluorapatite-catalyzed arylation4
Description (简体中文)
Other Notes
含不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reactant for preparation of biologically active molecules:
• Preparation of hydroxyphenylnaphthols as 17β-hydroxysteroid dehydrogenase Type 2 inhibitors1Reactant for:
• Preparation of axially-chiral biarylphosphonates by asymmetric Suzuki coupling catalyzed by palladium complexes with helically-chiral polyquinoxaline phosphine and polyphosphine copolymers2
• Preparation of arylpyrimidines and their use in regioselective acetoxylation3
• Preparation of N-arylated azoles via copper fluorapatite-catalyzed arylation4

REFERENCES