Superiority
2-Thiopheneboronic acid Basic information
Product Name: 2-Thiopheneboronic acid
Synonyms: TIMTEC-BB SBB004243;THIOPHENE-2-BORONIC ACID;THIOPHEN-2-YLBORONIC ACID;THIOPHENYL 2-BORONIC ACID;RARECHEM AH PB 0243;BUTTPARK 98\04-23;AKOS BRN-0022;2-THIENYLBORONIC ACID
CAS: 6165-68-0
MF: C4H5BO2S
MW: 127.96
EINECS:
Product Categories: Boron Compounds;Azoles;blocks;BoronicAcids;Boron, Nitrile, Thio,& TM-Cpds;Heterocycles;Substituted Boronic Acids;Boronic acids;Boronic Acid;Organoborons;Thiophene;B (Classes of Boron Compounds);organic or inorganic borate;Boronic Acids and Derivatives;Chemical Synthesis;Heteroaryl Boronic Acids;Organometallic Reagents;Boric Acid| Boric Acid Ester| Potassium Trifluoroborate
Mol File: 6165-68-0.mol
2-Thiopheneboronic acid Chemical Properties
mp 138-140 °C(lit.)
storage temp. 0-6°C
BRN 112375
CAS DataBase Reference 6165-68-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36/37-37/39-36
WGK Germany 3
Hazard Note Harmful/Irritant/Keep Cold
HazardClass IRRITANT, IRRITANT-HARMFUL, KEEP COLD
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
2-Thiopheneboronic acid Usage And Synthesis
Chemical Properties white to light yellow crystal powder
Usage Reagent used for• ;Palladium-catalyzed Suzuki-Miyaura cross-couplings1 • ;Alkylation, boration, coupling reaction, Suzuki coupling, and halogenation of fluorenyl bromide2 • ;Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer3 • ;Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters4 • ;Ligand-free Suzuki, Sonogashira, and Heck cross-coupling reactions5 • ;Copper-catalyzed nitration reactions6 • ;Geometry relaxation-induced Large Stokes shift in red-emitting borondipyrromethenes (BODIPY) and
Usage suzuki reaction
2-Thiopheneboronic acid Preparation Products And Raw materials
Preparation Products N-(4-THIOPHEN-2-YL-PHENYL)-ACETAMIDE
Details
2-Thiopheneboronic acid Basic information
Product Name: 2-Thiopheneboronic acid
Synonyms: TIMTEC-BB SBB004243;THIOPHENE-2-BORONIC ACID;THIOPHEN-2-YLBORONIC ACID;THIOPHENYL 2-BORONIC ACID;RARECHEM AH PB 0243;BUTTPARK 98\04-23;AKOS BRN-0022;2-THIENYLBORONIC ACID
CAS: 6165-68-0
MF: C4H5BO2S
MW: 127.96
EINECS:
Product Categories: Boron Compounds;Azoles;blocks;BoronicAcids;Boron, Nitrile, Thio,& TM-Cpds;Heterocycles;Substituted Boronic Acids;Boronic acids;Boronic Acid;Organoborons;Thiophene;B (Classes of Boron Compounds);organic or inorganic borate;Boronic Acids and Derivatives;Chemical Synthesis;Heteroaryl Boronic Acids;Organometallic Reagents;Boric Acid| Boric Acid Ester| Potassium Trifluoroborate
Mol File: 6165-68-0.mol
2-Thiopheneboronic acid Chemical Properties
mp 138-140 °C(lit.)
storage temp. 0-6°C
BRN 112375
CAS DataBase Reference 6165-68-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36/37-37/39-36
WGK Germany 3
Hazard Note Harmful/Irritant/Keep Cold
HazardClass IRRITANT, IRRITANT-HARMFUL, KEEP COLD
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
2-Thiopheneboronic acid Usage And Synthesis
Chemical Properties white to light yellow crystal powder
Usage Reagent used for• ;Palladium-catalyzed Suzuki-Miyaura cross-couplings1 • ;Alkylation, boration, coupling reaction, Suzuki coupling, and halogenation of fluorenyl bromide2 • ;Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer3 • ;Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters4 • ;Ligand-free Suzuki, Sonogashira, and Heck cross-coupling reactions5 • ;Copper-catalyzed nitration reactions6 • ;Geometry relaxation-induced Large Stokes shift in red-emitting borondipyrromethenes (BODIPY) and
Usage suzuki reaction
2-Thiopheneboronic acid Preparation Products And Raw materials
Preparation Products N-(4-THIOPHEN-2-YL-PHENYL)-ACETAMIDE
China (Mainland)
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