4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

HCID 2734620CAS 214360-73-3

Grundinformationen

Standard-SMILES
CC1(C)OB(c2ccc(N)cc2)OC1(C)C
InChIKey
ZANPJXNYBVVNSD-UHFFFAOYSA-N
Summenformel
C12H18BNO2
Durchschnittliche Molmasse
219,09 g/mol
Monoisotopische Masse
219,14305922

Namen und Bezeichner

Bevorzugter Name
4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
IUPAC
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Englischer Name
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Summenformel
C12H18BNO2
Molmasse
219.09

Namen und Synonyme

4-(tetramethyl-1,3,2-dioxaborolan-2-yl)anilineRefChem:516993629-061-7214360-73-34-Aminophenylboronic acid pinacol ester4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineMFCD020937214-Aminophenylboronic acid, pinacol ester(4-aminophenyl)boronic acid pinacol ester4-aminophenylboronic acid pinacolate4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine4-aminobenzeneboronic acid, pinacol ester
Weitere Namen anzeigen
4-Aminophenylboronic acid pinacol ester 97%4-(4,4,5,5-TetraMethyl-[1,3,2]dioxaborolan-2-yl)-phenylaMineCAS:214360-73-3BenzenaMine, 4-(4,4,5,5-te4-Aminophenylboronic acid pinacolTriamcinolone Acetonide Impurity 13
4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYLAMINE4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-aniline[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline; 2-(4-Aminophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 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-Aminophenylboronic Acid Pinacol Ester2-(4-AMINOPHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE;4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)ANILINE;4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-Y)ANILINE;4-AMINOPHENYLBORONIC ACID PINACOLATE;4-AMINOPHENYLBORONIC ACID PINACOL CYCLIC ESTER;4-AMPinacol cyclic esterBENZENAMINE, 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-SCHEMBL55445

Datenbank-Bezeichner

CAS
214360-73-3
PubChem CID
2734620
DTXSID
DTXSID30370400
EC Number
629-061-7
Nikkaji
J2.124.758H

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
44,5 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
1
Schwere Atome
16

Physikochemische Eigenschaften

Schmelzpunkt
165 · 165-169 °C (lit.)
Siedepunkt
340 · 340.0±25.0 °C(Predicted)
Dichte
1.05 · 1.05±0.1 g/cm3(Predicted)
storage temp.
Keep in dark place,Sealed in dry,Room Temperature
Löslichkeit
Chloroform
pka
4.24 · 4.24±0.10(Predicted)

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

Warning

H315 (97.9%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 47 reports by companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Hazard Classes and CategoriesSkin Irrit. 2 (97.9%)

Sicherheitsdaten

wgk
3
tsca
No
hs_code
29319090
risk_code
36/37/38
hazard_code
Xi
safety_code
26-36-37/39

Chemie und Industrie

Anwendungen · 2 Einträge

Beschreibung4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is an important organic reagent with an appearance ranging from white to yellow to orange powder to crystal. This compound can be used as a chemical reaction reagent or for preparing fluorescent probes.

Verwenden4-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.

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衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]

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