- 2-Thiopheneboronic acid
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- $0.00 / 25Kg/Drum
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2025-03-21
- CAS:6165-68-0
- Min. Order: 1Kg/Drum
- Purity: 99%
- Supply Ability: 5000KG
- 2-Thiopheneboronic acid
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- $8.00 / 1kg
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2024-04-23
- CAS:6165-68-0
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 2-Thiopheneboronic acid Basic information |
| | 2-Thiopheneboronic acid Chemical Properties |
| Melting point | 138-140 °C (lit.) | | Boiling point | 287.9±32.0 °C(Predicted) | | density | 1.32±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | Soluble in methanol. | | pka | 8.41±0.53(Predicted) | | form | Powder | | color | Off-white to beige | | BRN | 112375 | | Stability: | store cold | | InChIKey | ARYHTUPFQTUBBG-UHFFFAOYSA-N | | CAS DataBase Reference | 6165-68-0(CAS DataBase Reference) |
| 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 | | HS Code | 29339900 |
| | 2-Thiopheneboronic acid Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powder | | Uses | 2-Thiopheneboronic acid can be used as reagent used for Palladium-catalyzed Suzuki-Miyaura cross-couplings; Alkylation, boration, coupling reaction, Suzuki coupling, and halogenation of fluorenyl bromide ;Chain-growth catalyst transfer polycondensation of conjugated alternating copolymer; Ferric perchlorate-promoted reaction of fullerene to give fullerenyl boronic esters. | | Uses | 2-Thienylboronic Acid is a reagent used for palladium-catalyzed Suzuki-Miyaura cross-couplings. It is also used in preparation of photophysical properties of oxygen-containing polycyclic aromatic triptycenes. | | Uses | suzuki reaction |
| | 2-Thiopheneboronic acid Preparation Products And Raw materials |
| Preparation Products | 2,5-Dibromoterephthalic acid diethyl ester-->N-(4-THIOPHEN-2-YL-PHENYL)-ACETAMIDE-->1,3,5-tri(thiophen-2-yl)benzene-->3-(2-THIENYL)PYRIDINE-->4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole-->2-(2-THIENYL)PYRIDINE-->2-BENZOYLTHIOPHENE-->2,3'-bithiophene-5'-carbaldehyde-->6-Thien-2-ylnicotinaldehyde-->6-THIOPHEN-2-YL-1H-INDAZOLE-->4-Chloro-6-thiophen-2-yl-pyrimidine-->2,6-di(thiophen-2-yl)aniline-->(5-(THIOPHEN-2-YL)PYRIDIN-3-YL)METHANOL-->2-(thiophen-2-yl)pyridin-4-amine-->Pyrimidine, 2-chloro-4,6-di-2-thienyl- |
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