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| | 2-Aminophenylboronic acid pinacol ester Basic information |
| Product Name: | 2-Aminophenylboronic acid pinacol ester | | Synonyms: | 2-AMINOPHENYLBORONIC ACID, PINACOL CYCLIC ESTER;2-AMINOPHENYLBORONIC ACID, PINACOL ESTER;2-AMINOBENZENEBORONIC ACID PINACOL ESTER;2-Aminobenzeneboronic acid pinacol cyclic ester;-1,3,2-dioxaboroL;2-(4,4,5,5-TetramethyL;an-2-yL;2-Aminophenylboronic acid pinacol cyclic ester~2-(2-Aminophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | | CAS: | 191171-55-8 | | MF: | C12H18BNO2 | | MW: | 219.09 | | EINECS: | | | Product Categories: | Boronic Acid;Boronic acids;Substituted Boronic Acids;Amines;blocks;BoronicAcids;OLED | | Mol File: | 191171-55-8.mol |  |
| | 2-Aminophenylboronic acid pinacol ester Chemical Properties |
| Melting point | 63-68 °C (lit.) | | Boiling point | 125°C/1.5mmHg(lit.) | | density | 1.05±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | pka | 3.51±0.10(Predicted) | | form | Crystalline Powder | | color | Cream | | Water Solubility | Insoluble | | Sensitive | Air Sensitive | | BRN | 8548809 | | InChI | InChI=1S/C12H18BNO2/c1-11(2)12(3,4)16-13(15-11)9-7-5-6-8-10(9)14/h5-8H,14H2,1-4H3 | | InChIKey | ZCJRWQDZPIIYLM-UHFFFAOYSA-N | | SMILES | C1(N)=CC=CC=C1B1OC(C)(C)C(C)(C)O1 | | CAS DataBase Reference | 191171-55-8(CAS DataBase Reference) |
| Hazard Codes | Xi,Xn | | Risk Statements | 36/37/38-20/21/22 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 29310099 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 2-Aminophenylboronic acid pinacol ester Usage And Synthesis |
| Chemical Properties | cream crystalline powder | | Uses | Reactant involved in synthesis of: Indolo[3,4-cd]benzazepines via Pictet-Spengler-type cyclizations Antimicrobial amphiphilic aryl peptideomimetics Pyridoquinazolines and benzo[h] naphthyridines via intramolecular electrophilic substitution reaction | | Uses | Reactant involved in synthesis of:
- Indolo[3,4-cd][1]benzazepines via Pictet-Spengler-type cyclizations
- Antimicrobial amphiphilic aryl peptideomimetics
- Pyridoquinazolines and benzo[h][1,6]naphthyridines via intramolecular electrophilic substitution reactions
- Thienopyridine derivatives
- Dihydroquinolones
- Methacrylamidophenylboronic acids
| | Reactions | 2-Aminophenylboronic acid pinacol ester is a reactant involved in synthesis of:
Indolo[3,4-cd] benzazepines via Pictet-Spengler-type cyclizations
Antimicrobial amphiphilic aryl peptideomimetics
Pyridoquinazolines and benzo[h]naphthyridines via intramolecular electrophilic substitution reactions
Thienopyridine derivatives
Dihydroquinolones
Methacrylamidophenylboronic acids |
| | 2-Aminophenylboronic acid pinacol ester Preparation Products And Raw materials |
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