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4-Methyl-3-thienylboronic acid_Molecular_structure_CAS_177735-11-4)
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4-Methyl-3-thienylboronic acid

Catalog No. 542393 Name Sigma Aldrich
CAS Number 177735-11-4 Website http://www.sigmaaldrich.com
M. F. C5H7BO2S Telephone 1-800-521-8956
M. W. 141.98388 Fax
Purity ≥95% Email
Storage Chembase ID: 68625

SYNONYMS

Title
4-甲基-3-噻吩基硼酸
IUPAC name
(4-methylthiophen-3-yl)boronic acid
IUPAC Traditional name
4-methylthiophen-3-ylboronic acid
Synonyms
(4-Methylthien-3-yl)boronic acid
4-甲基-3-噻吩硼酸
4-Methyl-3-thiopheneboronic acid
(4-Methylthiophen-3-yl)boronic acid
(4-Methylthiophen-3-yl)dihydroxyborane

DATABASE IDS

CAS Number 177735-11-4
MDL Number MFCD04039882
PubChem SID 24878602

PROPERTIES

Empirical Formula (Hill Notation) C5H7BO2S
Purity ≥95%
Melting Point 138-144 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
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
Description (简体中文)
Analysis Note
最多可能含 1 当量的水
Other Notes
含不定量的酸酐。
包装
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

REFERENCES