missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Thiophene-2-boronic acid, 97%
CAS: 6165-68-0 | C4H5BO2S | 127.95 g/mol
$51.71 - $580.78
Chemical Identifiers
| CAS | 6165-68-0 |
|---|---|
| Molecular Formula | C4H5BO2S |
| Molecular Weight (g/mol) | 127.95 |
| MDL Number | MFCD00151850 |
| InChI Key | ARYHTUPFQTUBBG-UHFFFAOYSA-N |
| Synonym | thiophene-2-boronic acid, 2-thiopheneboronic acid, 2-thienylboronic acid, thienylboronic acid, 2-thiopheneboronicacid, thiophen-2-ylboranediol, thiophene2-boronic acid, thiophen-2-yl boronic acid, 2-thiophenylboric acid, boronic acid, thienyl |
| PubChem CID | 2733960 |
| IUPAC Name | thiophen-2-ylboronic acid |
| SMILES | OB(O)C1=CC=CS1 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|
AAB2307103
|
Thermo Scientific Chemicals
B2307103 |
1 g |
Each for $51.71
|
|
|||||
|
AAB2307106
|
Thermo Scientific Chemicals
B2307106 |
5 g |
Each for $135.77
|
|
|||||
|
AAB2307114
|
Thermo Scientific Chemicals
B2307114 |
25 g |
Each for $580.78
|
|
|||||
Description
Thiophene-2-boronic acid is a reagent used for Palladium-catalyzed Suzuki-Miyaura cross-couplings, Copper-catalyzed nitration reactions, Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer, Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters. It is also used in the preparation of Amino pyridine-based inhibitors of mitotic kinase Nek2 with potential antipoliferative effects in cancer tumors.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsThiophene-2-boronic acid is a reagent used for Palladium-catalyzed Suzuki-Miyaura cross-couplings, Copper-catalyzed nitration reactions, Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer, Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters. It is also used in the preparation of Amino pyridine-based inhibitors of mitotic kinase Nek2 with potential antipoliferative effects in cancer tumors.
Solubility
Soluble in methanol.
Notes
Store in a cool, dry conditions, in well sealed conditions. Store away from oxidizing agents.
Chemical Identifiers
| 6165-68-0 | |
| 127.95 | |
| ARYHTUPFQTUBBG-UHFFFAOYSA-N | |
| 2733960 | |
| OB(O)C1=CC=CS1 |
| C4H5BO2S | |
| MFCD00151850 | |
| thiophene-2-boronic acid, 2-thiopheneboronic acid, 2-thienylboronic acid, thienylboronic acid, 2-thiopheneboronicacid, thiophen-2-ylboranediol, thiophene2-boronic acid, thiophen-2-yl boronic acid, 2-thiophenylboric acid, boronic acid, thienyl | |
| thiophen-2-ylboronic acid |
Specifications
| 6165-68-0 | |
| C4H5BO2S | |
| 1 g | |
| thiophene-2-boronic acid, 2-thiopheneboronic acid, 2-thienylboronic acid, thienylboronic acid, 2-thiopheneboronicacid, thiophen-2-ylboranediol, thiophene2-boronic acid, thiophen-2-yl boronic acid, 2-thiophenylboric acid, boronic acid, thienyl | |
| ARYHTUPFQTUBBG-UHFFFAOYSA-N | |
| thiophen-2-ylboronic acid | |
| 2733960 | |
| 98% |
| 128°C to 131°C | |
| MFCD00151850 | |
| 112375 | |
| Soluble in methanol. | |
| OB(O)C1=CC=CS1 | |
| 127.95 | |
| 127.96 | |
| Thiophene-2-boronic acid |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
EINECSNumber : 000-000-0
TSCA : No
Recommended Storage : Keep cold
RUO – Research Use Only