Benzylcarbamat

Bezeichnung:Benzylcarbamat

CAS-Nr621-84-1

Englisch Name:Benzyl carbamate

CBNumberCB5100170

SummenformelC8H9NO2

Molgewicht151.16

MOL-Datei621-84-1.mol

Synonyma

Benzylcarbamat

Benzylcarbamat physikalisch-chemischer Eigenschaften

Schmelzpunkt	86-89 °C (lit.)
Siedepunkt	273.17°C (rough estimate)
Dichte	1.2023 (rough estimate)
Brechungsindex	1.5810 (estimate)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
Löslichkeit	Chloroform (Slightly), Methanol (Slightly)
pka	13.42±0.50(Predicted)
Aggregatzustand	Powder or Flakes
Farbe	Off-white to light beige
Wasserlöslichkeit	68.02g/L(37 ºC)
BRN	1865635
InChIKey	PUJDIJCNWFYVJX-UHFFFAOYSA-N
CAS Datenbank	621-84-1(CAS DataBase Reference)
NIST chemische Informationen	Carbamic acid, benzyl ester(621-84-1)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	20/21/22-36/37/38
S-Sätze:	22-24/25-36-26
WGK Germany	3
HS Code	29242995

Gefahreninformationscode (GHS)

Benzyl carbamate Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
Chemische Eigenschaften
Off-white to light beige powder or flakes, melting point 87-89 ℃. Insoluble in water, soluble in organic solvents such as benzene.
Application
Benzyl carbamate is an intermediate in the synthesis of various pharmaceutical compounds. It can be also used as nondeuterated internal standards for the quantitative analysis of carisoprodol in blood.
Verwenden
Benzyl carbamate is a reagent used for the nucleophilic introduction of an amino-protected group, Benzyl carbamates can be considered as a benzyloxycarbonyl (otherwise known as carbobenzyloxy, Cbz or Z) protecting group for amino groups. It was introduced as a versatile alternative to the ethoxy carbamate group in peptide synthesis.
synthetische
Benzyl carbamate is prepared by reacting benzyl chloroformate with ammonia. Benzyl chloroformate was slowly added to 5 times the volume of cold ammonia water (relative density 0.90) under vigorous stirring, the reaction mixture was placed at room temperature for 30 minutes, the precipitate was filtered out, washed with water and dried to obtain the finished product of benzyl carbamate.
läuterung methode
If it smells of NH3, then dry it in a vacuum desiccator and recrystallise it from 2 volumes of toluene and dry it in a vacuum desiccator again. It forms glistening plates from toluene, and can be recrystallised from H2O [Martell & Herbst J Org Chem 6 878 1941, Carter et al. Org Synth Coll Vol III 168 1955]. [Beilstein 6 IV 2278.]

Benzyl carbamate Upstream-Materialien And Downstream Produkte

Benzylcarbamat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

621-84-1, Benzyl carbamate Verwandte Suche:

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