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2,6-Dimethylphenylboronic acid_Molecular_structure_CAS_100379-00-8)
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2,6-Dimethylphenylboronic acid

Catalog No. 480061 Name Sigma Aldrich
CAS Number 100379-00-8 Website http://www.sigmaaldrich.com
M. F. C8H11BO2 Telephone 1-800-521-8956
M. W. 149.98274 Fax
Purity ≥95.0% Email
Storage Chembase ID: 32616

SYNONYMS

Title
2,6-二甲基苯硼酸
IUPAC name
(2,6-dimethylphenyl)boronic acid
IUPAC Traditional name
2,6-dimethylphenylboronic acid
Synonyms
2,6-Xyleneboronic acid
2,6-Dimethylbenzeneboronic acid
2,6-Xylylboronic acid

DATABASE IDS

PubChem SID 24871544
MDL Number MFCD01009693
CAS Number 100379-00-8

PROPERTIES

Impurities <10% water
Linear Formula (CH3)2C6H3B(OH)2
Purity ≥95.0%
Melting Point 105 °C (dec.)(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
5, 25 g in glass bottle
Application
Reagent used for
• Palladium catalyzed Suzuki-Miyaura coupling reactions1
• One-pot ipso-nitration of arylboronic acids including broader substrate scope of heterocycles and functional groups2
• Nickel-Catalyzed Cross-Coupling of Chromene Acetals and Boronic Acids3
• Visible-light initiated aerobic oxidative hydroxylation catalyzed by Ru-complex4
• Rhodium(I)-catalyzed 1,4-addition reactions5
• Pd-catalyzed homocouplings6
• Expanded scope of Cu assisted Suzuki-Miyaura coupling reactions including aryl chlorides and polyhalo aryl boronates7 Reagent used in Prepration of
• Orally bioavialable G Protein-Coupled Receptor 40 agonists for diabetes treatment8
• Solid phase synthesis and antitumor structure-activity relationship of Smac triazoloprolines and biarylalanines tetrapeptide libraries9
• Protein Kinase inhibitors10
Description (简体中文)
Other Notes
含不定量的酸酐
包装
5, 25 g in glass bottle
Application
Reagent used for
• Palladium catalyzed Suzuki-Miyaura coupling reactions1
• One-pot ipso-nitration of arylboronic acids including broader substrate scope of heterocycles and functional groups2
• Nickel-Catalyzed Cross-Coupling of Chromene Acetals and Boronic Acids3
• Visible-light initiated aerobic oxidative hydroxylation catalyzed by Ru-complex4
• Rhodium(I)-catalyzed 1,4-addition reactions5
• Pd-catalyzed homocouplings6
• Expanded scope of Cu assisted Suzuki-Miyaura coupling reactions including aryl chlorides and polyhalo aryl boronates7 Reagent used in Prepration of
• Orally bioavialable G Protein-Coupled Receptor 40 agonists for diabetes treatment8
• Solid phase synthesis and antitumor structure-activity relationship of Smac triazoloprolines and biarylalanines tetrapeptide libraries9
• Protein Kinase inhibitors10

REFERENCES