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HCID 201622Erstellt: 3. November 2026

Diiodotriphenylphosphorane

TRIPHENYLPHOSPHINE DIIODIDE · DIIDOTRIPHENYLPHOSPHORANE · diiodotriphenyl-phosphoran · DIIODOTRIPHENYLPHOSPHORANE · Triphenyldiiodophosphorane · Phosphorane, diiodotriphenyl- · iodotriphenylphosphoraniumiodide · diiodo(triphenyl)-$l^{5}-phosphane

https://huagongshe.com/de/chemical/201622

Molekülstruktur von Diiodotriphenylphosphorane

Identifikatoren & physikalische Daten

CAS No.6396-07-2
SummenformelC18H15I2P
Durchschnittliche Molmasse516,1 g/mol
Monoisotopische Masse515,90008 g/mol
SMILESIP(I)(c1ccccc1)(c1ccccc1)c1ccccc1
InChIKeyNSWZEXJQHIXCFL-UHFFFAOYSA-N
PubChem CID201622
EC No.627-787-9
DTXSIDDTXSID70213802

Chemische & physikalische Eigenschaften

XLogP6,3
Polarare Oberfläche (TPSA)0
H-Brücken-Donoren0
H-Brücken-Akzeptoren0
Frei drehbare Bindungen3
Schwere Atome21
Formalladung0
Komplexität285
Schmelzpunkt210-220 °C (lit.)
Lagerbedingungen2-8°C
AggregatzustandPowder
FarbeYellow to orange
InChI1S/C18H15I2P/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChIKeyNSWZEXJQHIXCFL-UHFFFAOYSA-N
SMILESIP(I)(c1ccccc1)(c2ccccc2)c3ccccc3
CAS Datenbank6396-07-2

Sicherheit & Vorschriften

GHS-EinstufungDangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P203, P233, P260, P261, P264, P271, P272, P280, P284, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P318, P321, P333+P317, P342+P316, P362+P364, P363, P403, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Corr. 1B (100%)
F8-10
Wassergefährdungsklasse (WGK)3
UN-TransportnummerUN 2923 8/PG 2
RTECS-Nr.TB6100000
R-Sätze (R)34-42/43-62
GefahrensymboleC
Sicherheitshinweise (S)26-36/37/39-45
Gefahrenklasse8Eye Dam. 1Repr. 2Resp. Sens. 1Skin Corr. 1BSkin Sens. 1
Lagerklasse8A - Combustible corrosive hazardous materials

Anwendungen & Verwendung

Verwenden

Triphenylphosphine diiodide (Ph3P. I2) can be used as a reagent: To facilitate the conversion of alcohol, thiol, and enol functional groups into alkyl iodides via formation of alkoxyphosphonium iodide. To prepare β-iodo-α,β-unsaturated ketones from cyclic β-diketones in the presence of triethyl amine. In the synthesis of alkyl nitrates from alcohols. In the Beckmann rearrangement reaction to synthesize lactams from cycloalkanone oxime. For the preparation of aromatic and aliphatic carboxylic acid esters in the presence of N,N-dimethylaminopyridine. Ph3P. I2 can also be used to reduce graphene oxide for the production of graphene nanosheets under mild and environmentally friendly conditions.