4-tert-Butoxystyrene

4-tert-Butoxystyrene Struktur
95418-58-9
CAS-Nr.
95418-58-9
Englisch Name:
4-tert-Butoxystyrene
Synonyma:
P-T-BUTOXYSTYRENE;4-T-BUTOXYSTYRENE;p-tert-butoxystyrene;1-ethenyl;butoxy styrene;4-tert-butoxystyene;4-TERT-BUTOXYSTYRENE;(1-Butoxyvinyl)benzene;4-tert-Butyloxystyrene;p-(tert-Butyloxy)styrene
CBNumber:
CB6229094
Summenformel:
C12H16O
Molgewicht:
176.25
MOL-Datei:
95418-58-9.mol

4-tert-Butoxystyrene Eigenschaften

Schmelzpunkt:
−38 °C(lit.)
Siedepunkt:
256.8±9.0 °C Press: 760 Torr
Dichte
0.936 g/mL at 25 °C(lit.)
Dampfdruck
17.999Pa at 20℃
Brechungsindex
n20/D 1.524(lit.)
Flammpunkt:
207 °F
InChI
InChI=1S/C12H16O/c1-5-10-6-8-11(9-7-10)13-12(2,3)4/h5-9H,1H2,2-4H3
InChIKey
GRFNSWBVXHLTCI-UHFFFAOYSA-N
SMILES
C1(OC(C)(C)C)=CC=C(C=C)C=C1
LogP
3.83 at 22℃ and pH7
CAS Datenbank
95418-58-9(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 36/37/38
S-Sätze: 26-36
WGK Germany  3
HS Code  2902900000
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P271 Nur im Freien oder in gut belüfteten Räumen verwenden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P302+P352 BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckmäßig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.

4-tert-Butoxystyrene Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Beschreibung

4-tert-butoxystyrene is a pendant functionalized styrene that structurally, It is similar to PMOS, both carrying an alkoxyl p-substituent, whose electron-donating and resonance effects allow them to be'polymerized by cationic, anionic, and radical mechanisms. It is used to treatment of its polymers with an acid leads to poly(4-vinylphenol), which finds a wide variety of applications to photoresists, epoxy-curing agents, adhesives, etc.).

Chemische Eigenschaften

Colorless to Almost colorless clear liquid.

Verwenden

4-tert-Butoxystyrene is used in organic synthesis. It is used to synthesize 4'-tert-butoxy-biphenyl-4-carboxylic acid methyl ester.

Synthese

Preparation of 4-tert-Butoxystyrene (3-tert-Butoxystyrene). To a 2000-mL three-necked round-bottom flask equipped with a dropping funnel, thermometer, reflux condenser, paddle stirrer and nitrogen inlet were placed 19.4 g (0.80 mol) of magnesium turnings and enough freshly dried and distilled tetrahydrofuran (THF) to cover the turnings. There were then added dropwise with stirring a solution of 143.3g (0.78 mol) of freshly distilled 4-bromostyrene (bp 46-47°C (0.03 mm)) in 500mL of THF. After 20mL of the 4-bromostyrene had been added, an exothermic reaction set in and was maintained between 25 and 35°C by adjusting the rate of addition of the bromo compound and with the aid of an ice bath. After the addition had been completed, the reaction mixture was heated to 60°C for 0.5h. Using a NaC1-ice bath, the mixture was cooled to 0°C and a solution of 100.88g (0.52 mol) of tert-butyl peroxybenzoate in 200 mL of THF was added via the dropping funnel at such a rate that the reaction temperature was maintained between 0 and 5°C. After completion of the addition, the reaction mixture was stirred at 25°C for 2 h. The organic layer was separated from the solid magnesium benzoate by decantation and the volume of the solution reduced on a rotary evaporator. The yellow oil that remained was washed with 1000 mL of 3% aqueous HCl solution and the organic layer separated. The aqueous layer was washed with two 200-mL portions of ether, and the ether and organic layers were combined and together washed with two 75-mL portions of a 10% NaOH solution followed by washing with water until the aqueous washings were neutral. After the solution was dried over Na2S04 and the ether was removed via a rotary evaporator, the remaining pale yellow oil was purified by fractional distillation in the presence of a few milligrams of ionol (2,6-ditert-butyl-4-methylphenol) as an inhibitor. There were obtained 46 g (50% yield, bp 45°C (0.02 mm)) of 4-tert-Butoxystyrene having the following elemental analysis.

4-tert-Butoxystyrene Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


4-tert-Butoxystyrene Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 128)Lieferanten
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95418-58-9()Verwandte Suche:


  • 4-TERT-BUTOXYSTYRENE
  • 1-Vinyl-4-(tert-butyloxy)benzene
  • 4-(tert-Butyloxy)styrene
  • 4-tert-Butyloxystyrene
  • p-(tert-Butyloxy)styrene
  • tert-Butyl(4-vinylphenyl) ether
  • (1-Butoxyethenyl)benzene
  • (1-Butoxyvinyl)benzene
  • Butyl 1-phenylethenyl ether
  • T-BUTYL=P-VINYLPHENYL=ETHER
  • tert-Butyl p-vinylphenyl ether
  • butoxy styrene
  • 4-tert-butoxystyene
  • 4-tert-Butoxystyrene 99%, contains 200 ppM 4-tert-butylcatechol as inhibitor
  • 1-ethenyl-4-[(2-methylpropan-2-yl)oxy]benzene
  • 1-(tert-Butoxy)-4-ethenylbenzene
  • Benzene, 1-(1,1-dimethylethoxy)-4-ethenyl-
  • 4-tert-Butoxystyrene (stabilized with TBC)
  • 1-Vinyl-4-(tert-butyloxy)benzene(PTBS)
  • ppm 4-tert-butylcatechol as inhibitor
  • P-T-BUTOXYSTYRENE
  • p-tert-butoxystyrene
  • 4-T-BUTOXYSTYRENE
  • 1-ethenyl
  • 95418-58-9
  • H2CCHC6H4OCCH33
  • Monomers
  • Polymer Science
  • Styrene and Functionalized Styrene Monomers
  • Aromatic compound
  • monomer
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