Dibenzylcarbonat

DIBENZYL CARBONATE Struktur
3459-92-5
CAS-Nr.
3459-92-5
Bezeichnung:
Dibenzylcarbonat
Englisch Name:
DIBENZYL CARBONATE
Synonyma:
Benzyl carbonate;NSC 406789;DIBENZYL CARBONATE;dibenzyl carbazate;Dibenzylcarbonate,98%;Linezolid Impurity 50;Dibenzyl Carbonate >Dibenzyl carbonate 99%;CARBONIC ACID DIBENZYL ESTER;Carbonic acid, bis(phenylmethyl) ester
CBNumber:
CB5677478
Summenformel:
C15H14O3
Molgewicht:
242.27
MOL-Datei:
3459-92-5.mol

Dibenzylcarbonat Eigenschaften

Schmelzpunkt:
29-33 °C(lit.)
Siedepunkt:
180-190 °C2 mm Hg(lit.)
Dichte
1.1515 (rough estimate)
Brechungsindex
1.5485
Flammpunkt:
>230 °F
Löslichkeit
Sparingly Soluble (0.099 g/L) (25°C).
Aggregatzustand
powder to lump
Farbe
White to Almost white
Sensitive 
Air Sensitive
BRN 
1882864
CAS Datenbank
3459-92-5(CAS DataBase Reference)
EPA chemische Informationen
Carbonic acid, bis(phenylmethyl) ester (3459-92-5)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn
R-Sätze: 21/22
S-Sätze: 36
WGK Germany  3
TSCA  Yes
HS Code  29209090
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H312 Gesundheitsschädlich bei Hautkontakt. Akute Toxizität dermal Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P280,P302+P352, P312, P322, P363,P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P321 Besondere Behandlung
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Dibenzylcarbonat Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R21/22:Gesundheitsschädlich bei Berührung mit der Haut und beim Verschlucken.

S-Sätze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Chemische Eigenschaften

Colorless low melting solid

Verwenden

Ionic liquids can effectively accelerate slow N-benzylation reactions utilizing dibenzyl carbonate as an alkylating reagent. Dibenzyl carbonate (DBzlC) has been used to benzylate phenylacetonitrile, benzyl phenylacetate and phenol. Selective N, N-dibenzylation of primary aliphatic amines was carried with dibenzyl carbonate in the presence of phosphonium salts.

synthetische

To a stirred solution of benzyl alcohol (0.216 g, 2.00 mol), tributylphosphine (0.303 g, 1.50 mmol), and CyTMG (0.394 g, 2.00 mmol) in DMF (2.00 mL), CO2 was added at room temperature. After 15 min, tetrabromomethane (0.663 g, 2.00 mmol) was added, the reaction vessel was sealed, and the contents were stirred for 2 h. Thereafter, the reaction mixture was diluted with ethyl acetate, washed successively with 0.5 m aqueous HCl and saturated aq. NaHCO3 solution, and dried over Na2SO4. Diphenylmetha- nol was added to the organic solution as an internal standard and the yield of dibenzyl carbonate was determined from the relative integrals of a methylene peak of the carbonate and a methine peak of diphenylmethanol in the 1H NMR spectrum of the ethyl acetate solution. Dibenzyl carbonate, prepared by a larger scale reaction of CO2 with benzyl alcohol (1.08 g, 10.0 mmol), was isolated by column chromatography (cyclohexane/ethyl acetate, 50:1) in 67.3% yield (0.816 g).

Allgemeine Beschreibung

Dibenzyl carbonate (DBC) is commonly used as a benzylating agent. Dimethyl carbonate and excess of benzyl alcohol undergoes transesterification in the presence of CsF/α-Al2O3 (cesium fluoride/aluminum oxide) to form DBC. The formation of N,N-dibenzyl derivatives by the reaction of primary aliphatic amines with DBC in the presence of phosphonium salts has been investigated.

Dibenzylcarbonat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Dibenzylcarbonat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 138)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5993 58
career henan chemical co
+86-0371-86658258 15093356674;
factory@coreychem.com China 29826 58
Aston Chemical
13000000000
sales@astonchem.com United States 1634 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739
info@dycnchem.com CHINA 52867 58
Labnetwork lnc.
+86-27-50766799 +8618062016861
contact@labnetwork.com China 19994 58
Alfa Chemistry
+1-5166625404
Info@alfa-chemistry.com United States 21317 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923
1026@dideu.com China 9116 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207
sales@molcore.com China 49739 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503259 +86-19930503259
cherry@crovellbio.com China 18456 58
PT CHEM GROUP LIMITED
+86-85511178 +86-85511178
peter68@ptchemgroup.com China 35453 58

3459-92-5(Dibenzylcarbonat)Verwandte Suche:


  • Carbonic acid, bis(phenylmethyl) ester
  • CARBONIC ACID DIBENZYL ESTER
  • DIBENZYL CARBONATE
  • Dibenzylcarbonate,98%
  • dibenzyl carbazate
  • NSC 406789
  • Dibenzyl carbonate 99%
  • Linezolid Impurity 50
  • Dibenzyl Carbonate >
  • Benzyl carbonate
  • 3459-92-5
  • 3459-92-6
  • C6H5CH2O2CO
  • Carbonates
  • Carbonyl Compounds
  • Building Blocks
  • Protection & Derivatization Reagents (for Synthesis)
  • Organic Building Blocks
  • Protection & Derivatization Reagents (for Synthesis)
  • Synthetic Organic Chemistry
  • Carbonates
  • Carbonyl Compounds
  • Organic Building Blocks
Copyright 2019 © ChemicalBook. All rights reserved