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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 87774Erstellt: 26. Oktober 2026

Tribenzylchlorsilan

CHLOROTRIBENZYLSILANE · TRIBENZYL CHLOROSILANE · TRIBENZYLSILYL CHLORIDE · tribenzylchlorosilicane · Tribenzylchlorosilane 97% · chlorotris(phenylmethyl)-silan · Chlorotris(phenylmethyl)silane · Tribenzylchlorosilane, Tribenzylsilyl chloride

https://huagongshe.com/de/chemical/87774

Molekülstruktur von Tribenzylchlorsilan

Identifikatoren & physikalische Daten

CAS No.18740-59-5
SummenformelC21H21ClSi
Durchschnittliche Molmasse336,9 g/mol
Monoisotopische Masse336,11010488 g/mol
SMILESCl[Si](Cc1ccccc1)(Cc1ccccc1)Cc1ccccc1
InChIKeyUTXPCJHKADAFBB-UHFFFAOYSA-N
PubChem CID87774
EC No.242-549-0
DTXSIDDTXSID0066404
Lokaler NameTribenzylchlorsilan

Chemische & physikalische Eigenschaften

Polarare Oberfläche (TPSA)0
H-Brücken-Donoren0
H-Brücken-Akzeptoren0
Frei drehbare Bindungen6
Schwere Atome23
Formalladung0
Komplexität274
Schmelzpunkt139-142 °C(lit.)
Siedepunkt437.9±14.0 °C(Predicted)
Dichte1.096±0.06 g/cm3(Predicted)
Löslichkeitsparingly sol cold petroleum ethermoderately sol hot petroleum ethersol ether.
EPA chemische InformationenSilane, chlorotris(phenylmethyl)- (18740-59-5)

Sicherheit & Vorschriften

GHS-EinstufungDangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Corr. 1B (100%)
F10-21
Wassergefährdungsklasse (WGK)3
TSCA-Inventar-StatusTSCA listed
UN-TransportnummerUN 3261 8/PG 2
R-Sätze (R)34
GefahrensymboleC
Sicherheitshinweise (S)26-36/37/39-45
Gefahrenklasse8
VerpackungsgruppeII

Anwendungen & Verwendung

Verwenden

Tribenzylchlorosilane is widely used as reagent for alcohol protection.

Herstellung & Synthese

synthetische

It is prepared by reaction of benzylmagnesium chloride with SiCl4 in ether; separation from mono- and dibenzylated chlorosilane byproducts is then accomplished by fractional distillation (boiling range 300–360 °C/100 mmHg). Other preparations involve the chlorination of tribenzylsilane using Cl2 or an acyl chloride. No yields are reported for any of the above preparative procedures.