Substance
ID:314675
Names and Identifiers
IUPAC Traditional name
4-methylthiophen-3-ylboronic acid
IUPAC name
(4-methylthiophen-3-yl)boronic acid
Synonyms
4-Methyl-3-thiopheneboronic acid4-甲基-3-噻吩硼酸(4-Methylthien-3-yl)boronic acid(4-Methylthiophen-3-yl)boronic acid4-Methyl-3-thienylboronic acid4-甲基-3-噻吩基硼酸(4-Methylthiophen-3-yl)dihydroxyborane
Properties
Safety Information
MSDS Link
Storage Temperature
2-8°C
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Physical Property
Melting Point
138-144 °C(lit.)
Product Information
Purity
≥95%
Empirical Formula (Hill Notation)
C5H7BO2S
Molecule Details
Analysis Note
May contain up to 1 equivalent of water
Other Notes
Contains varying amounts of anhydride.
Packaging
1 g in glass bottle
Application
Reactant for preparation of biologically active molecules:
• Selective sphingosine phosphate receptor antagonists1
• Biarylimidazole derivatives as H+/K+ ATPase inhibitors2
• Benzothienopyrimidinones as inhibitors of human protooncogene proviral insertion site in moloney murine leukemia virus kinases3Used in:
• Synthesis of arene-functionalized fullerenes via rhodium-catalyzed hydroarylation4
• Suzuki cross-coupling reactions5
May contain up to 1 equivalent of water
Other Notes
Contains varying amounts of anhydride.
Packaging
1 g in glass bottle
Application
Reactant for preparation of biologically active molecules:
• Selective sphingosine phosphate receptor antagonists1
• Biarylimidazole derivatives as H+/K+ ATPase inhibitors2
• Benzothienopyrimidinones as inhibitors of human protooncogene proviral insertion site in moloney murine leukemia virus kinases3Used in:
• Synthesis of arene-functionalized fullerenes via rhodium-catalyzed hydroarylation4
• Suzuki cross-coupling reactions5
Molecular Spectra
No Data Available
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References
No Data Available
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