Ethyltrimethylsilylacetat

Ethyl (trimethylsilyl)acetate Struktur
4071-88-9
CAS-Nr.
4071-88-9
Bezeichnung:
Ethyltrimethylsilylacetat
Englisch Name:
Ethyl (trimethylsilyl)acetate
Synonyma:
ETSA;2-trimethylsilylbutanoate;Ethyl(Trimethylsily)Acetate;ETHYL (TRIMETHYLSILYL)ACETATE;ETHYL(2-TRIMETHYLSILYL)ACETATE;ETHYL TRI METHYLSILYLACETATE 99%;Ethyl (trimethylsilyl)acetate,97%;Ethyl acetatethree Methylsilicone;Ethyl (trimethylsilyl)acetate, 98+%;(TRIMETHYLSILYL)ACETIC ACID ETHYL ESTER
CBNumber:
CB7271085
Summenformel:
C7H16O2Si
Molgewicht:
160.29
MOL-Datei:
4071-88-9.mol

Ethyltrimethylsilylacetat Eigenschaften

Siedepunkt:
156-159 °C (lit.)
Dichte
0.876 g/mL at 25 °C (lit.)
Brechungsindex
n20/D 1.415(lit.)
Flammpunkt:
95 °F
storage temp. 
Inert atmosphere,Room Temperature
Löslichkeit
sol ethereal and chlorinated solvents; reacts with protic solvents.
Aggregatzustand
clear liquid
Farbe
Colorless to Almost colorless
Wichte
0.876
Wasserlöslichkeit
Decomposition
Hydrolytic Sensitivity
2: reacts with aqueous acid
Sensitive 
Moisture Sensitive
BRN 
1755902
CAS Datenbank
4071-88-9(CAS DataBase Reference)
NIST chemische Informationen
Ethyl (trimethylsilyl)acetate(4071-88-9)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
R-Sätze: 10
S-Sätze: 16-24/25
RIDADR  UN 3272 3/PG 3
WGK Germany  3
10-21
TSCA  Yes
HazardClass  3
PackingGroup  III
HS Code  29319090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H226 Flüssigkeit und Dampf entzündbar. Entzündbare Flüssigkeiten Kategorie 3 Warnung
Sicherheit
P210 Von Hitze, heißen Oberflächen, Funken, offenen Flammen und anderen Zündquellenarten fernhalten. Nicht rauchen.
P240 Behälter und zu befüllende Anlage erden.
P241 Explosionsgeschützte [elektrische/Lüftungs-/ Beleuchtungs-/...] Geräte verwenden.
P303+P361+P353 BEI BERÜHRUNG MIT DER HAUT (oder dem Haar): Alle kontaminierten Kleidungsstücke sofort ausziehen. Haut mit Wasser abwaschen oder duschen.

Ethyltrimethylsilylacetat Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R10:Entzündlich.

S-Sätze Betriebsanweisung:

S16:Von Zündquellen fernhalten - Nicht rauchen.

Chemische Eigenschaften

Ethyl trimethylsilylacetate is a clear colorless liquid. It is stable to the usual manipulations, and can be stored in glass containers for years without change of physical and spectral properties.

Verwenden

Ethyl trimethylsilylacetate is used in the synthesis of ethyl-2,2-dibromo-2-(trimethylsilyl)acetate and α,β-unsaturated esters. It was also used to silylate the enolizable aldehydes and ketones.

synthetische

ethyl trimethylsilylacetate synthesis: Available by a Reformatsky reaction from ethyl bromoacetate, and by reaction of trimethylsilylmethylmagnesium chloride with ethyl chloroformate. An alternative approach requires the treatment of ethyl acetate with triphenylmethylsodium followed by chlorotrimethylsilane The use of a nitrogen base with ethyl acetate in THF followed by reaction with chlorotrimethylsilane results in a mixture of C- and O-silylation. The use of HMPA as additive in the reaction medium increases the amount of O-silylation to 90%. Similar methods can be used to prepare analogs.

Allgemeine Beschreibung

Reaction of ethyl trimethylsilylacetate (ETSA) with dilute hydrochloric acid, dilute alkali, anhydrous HCl, anhydrous bromine and absolute ethanol has been reported. ETSA undergoes condensation with aromatic aldehydes in the presence of base catalyst to yield β-trimethylsiloxycarboxylates. Lithium ETSA reacts with ketones to yield α,β-unsaturated esters.

läuterung methode

Purify it by distilling ca 10g of reagent through a 15cm, Vigreux column (p 11) and then redistilling it through a 21cm glass helices-packed column [Hauze & Hauser J Am Chem Soc 75 994 1953]. Alternatively, dissolve it in Et2O, wash with H2O, dilute Na2CO3, dry over Na2CO3, evaporate Et2O, and distil it through a column of 15 theoretical plates. [Gold et al. J Am Chem Soc 70 2874 1948, Beilstein 4 IV 3974.]

Ethyltrimethylsilylacetat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Ethyltrimethylsilylacetat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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4071-88-9(Ethyltrimethylsilylacetat)Verwandte Suche:


  • ETHYL(2-TRIMETHYLSILYL)ACETATE
  • ETHYL (TRIMETHYLSILYL)ACETATE
  • (TRIMETHYLSILYL)ACETIC ACID ETHYL ESTER
  • ETHYL TRI METHYLSILYLACETATE 99%
  • Ethyl(Trimethylsily)Acetate
  • ETSA~(Trimethylsilyl)acetic acid ethyl ester
  • Ethyl (trimethylsilyl)acetate, 98+%
  • 2-(Trimethylsilyl)acetic acid ethyl ester
  • 2-[Dimethyl(methyl)silyl]acetic acid ethyl ester
  • Ethyl (trimethylsilyl)acetate,97%
  • (Trimethylsilyl)acetic Acid Ethyl Ester ETSA
  • Ethyl acetatethree Methylsilicone
  • Acetic acid, (trimethylsilyl)-, ethyl ester
  • ETHYL 2-(TRIMETHYLSILYL)ACETATE, 97%ETHYL 2-(TRIMETHYLSILYL)ACETATE, 97%ETHYL 2-(TRIMETHYLSILYL)ACETATE, 97%
  • 2-trimethylsilylbutanoate
  • TIANFUCHEM-- 4071-88-9--Ethyl (trimethylsilyl)acetate in stock
  • ETSA
  • 4071-88-9
  • C7H16O2Si
  • CH33SiCH2CO2CH2CH3
  • CH33SiCH2CO2C2H5
  • Carbonyl Compounds
  • C6 to C7
  • Building Blocks
  • Si (Classes of Silicon Compounds)
  • Silicon Compounds (for Synthesis)
  • Si-(C)4 Compounds
  • Organic Building Blocks
  • Esters
  • Si (Classes of Silicon Compounds)
  • Si-(C)4 Compounds
  • Silicon Compounds (for Synthesis)
  • Synthetic Organic Chemistry
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