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| | 4-Carbamoylphenylboronic acid Basic information |
| | 4-Carbamoylphenylboronic acid Chemical Properties |
| Melting point | 242-252°C | | Boiling point | 414.3±47.0 °C(Predicted) | | density | 1.32±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | soluble in Methanol | | form | powder or crystals | | pka | 7.87±0.10(Predicted) | | color | white to off-white | | InChI | 1S/C7H8BNO3/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4,11-12H,(H2,9,10) | | InChIKey | GNRHNKBJNUVWFZ-UHFFFAOYSA-N | | SMILES | NC(=O)c1ccc(cc1)B(O)O | | CAS DataBase Reference | 123088-59-5(CAS DataBase Reference) |
| Hazard Codes | C,Xi,Xn | | Risk Statements | 36/37/38-22-20/21/22 | | Safety Statements | 26-36/37/39-36-24/25 | | WGK Germany | 3 | | Hazard Note | Corrosive | | TSCA | No | | HazardClass | IRRITANT | | HS Code | 29310095 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| | 4-Carbamoylphenylboronic acid Usage And Synthesis |
| Chemical Properties | White to brown solid | | Uses | Reactant involved in:
- Suzuki-Miyaura, Sonogashira and Buchwald-Hartwig cross-coupling reactions for the synthesis of substituted pyrene derivatives
- Suzuki-Miyaura reactions for the synthesis of aryl-substituted oxabenzindoles and methanobenzindoles or 2-aminoimidazole triazoles
- Three-component coupling with triflates and alkenes
Reactant involved in synthesis of biologically active molecules including:
- Hybrid peptidomimetic molecules as STAT3 protein inhibitors
- Vasopressin V1B receptor antagonists for use as antidepressants oand anxiolytics
- (Thienopyridine)caboxamides as CHK1 inhibitors
| | Uses | suzuki reaction |
| | 4-Carbamoylphenylboronic acid Preparation Products And Raw materials |
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