Product

4-Aminophenylboronic acid pinacol ester

CAS No.：214360-73-3

Other grades of this product :

4-Aminophenylboronic acid pinacol ester Basic information

Product Name:	4-Aminophenylboronic acid pinacol ester
Synonyms:	2-(4-AMINOPHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE;4-Aminophenylboronic acid pinacol ester 97%;4-Aminophenylboronic acid picol ester;4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, 2-(4-Aminophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;BenzenaMine, 4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;4-Aminophenylboronic acid pinacol ester 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline;4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzeneamine;4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZENAMINE
CAS:	214360-73-3
MF:	C12H18BNO2
MW:	219.09
EINECS:	629-061-7
Product Categories:	organic or inorganic borate;B (Classes of Boron Compounds);Substituted Boronic Acids;Boronic Acid;Boronic Acids Esters;CHIRAL CHEMICALS;Boron compounds
Mol File:	214360-73-3.mol

4-Aminophenylboronic acid pinacol ester Chemical Properties

Melting point	165-169 °C (lit.)
Boiling point	340.0±25.0 °C(Predicted)
density	1.05±0.1 g/cm3(Predicted)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
solubility	Chloroform
pka	4.24±0.10(Predicted)
form	Crystalline Powder
color	Almost white to light beige
Water Solubility	Insoluble
InChIKey	ZANPJXNYBVVNSD-UHFFFAOYSA-N
CAS DataBase Reference	214360-73-3(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36-37/39
WGK Germany	3
TSCA	No
HazardClass	IRRITANT
HS Code	29319090

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English

4-Aminophenylboronic acid pinacol ester Usage And Synthesis

Chemical Properties	almost white to light beige crystalline powder
Uses	suzuki reaction
Uses	4-Aminophenylboronic acid pinacol ester can be used as a reagent for: The preparation of substituted 3-phenyl-4H-1-benzopyran-4-ones by reacting with iodochromones via Pd catalyzed Suzuki-Miyaura cross-coupling reaction. Mercury(II) detection by fluorometry with new fluorogenic indicators based on through-bond energy transfer from pentaquinone to rhodamine. Rhodium-catalyzed amination reactions. Palladium-catalyzed Suzuki cross-coupling to synthesize potential antitubercular and antimicrobial compounds. It can also be used to prepare: Hexaphenylbenzene derivatives as a potential bioprobe and multichannel keypad system. Pyromellitic diimide-based polymer as matrix for solution-processable n-channel field-effect transistors. Alternating copolymers of oligoarylenes and naphthalene bisimides as low band-gap semiconductors with electrochemical and spectroelectrochemical behavior. γ-secretase modulators in the treatment of amyloid β formation.

4-Aminophenylboronic acid pinacol ester Preparation Products And Raw materials

Raw materials	Triethylamine-->1,4-Dioxane-->Palladium (II) Acetate-->4-Bromoaniline-->(OXYDI-2,1-PHENYLENE)BIS(DIPHENYLPHOSPHINE)-->Pinacolborane
Preparation Products	4-Aminophenylboronic acid-->4-(N-METHYLAMINO)PHENYLBORONIC ACID, PINACOL ESTER-->4'-(4-AMINOPHENYL)-2,2':6',2''-TERPYRIDINE-->4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER-->4-(METHYLSULFONYLAMINO)PHENYLBORONIC ACID-->4,4''-DIAMINO-P-TERPHENYL

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