Grundinformationen
- Standard-SMILES
C[Si](C)(C)I- InChIKey
CSRZQMIRAZTJOY-UHFFFAOYSA-N- Summenformel
- C3H9ISi
- Durchschnittliche Molmasse
- 200,09 g/mol
- Monoisotopische Masse
- 199,95182482
Überblick
structure in first source
Namen und Bezeichner
- Bevorzugter Name
- Trimethylsilyl iodide
- IUPAC
- iodo(trimethyl)silane
- Lokaler Name
- Iodotrimethylsilan
- Englischer Name
- Iodotrimethylsilane
- Summenformel
- C3H9ISi
- Molmasse
- 200.09
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
16029-98-4- PubChem CID
- 85247
- DTXSID
DTXSID4065997- UNII
- 7A65KRZ6NV
- EC Number
- 240-171-0
- Nikkaji
- J150.775C
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 0
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 5
- Formalladung
- 0
- Komplexität
- 28,4
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 0 °C · <0°C
- Siedepunkt
- 106 °C · 106 °C(lit.)
- Dichte
- 1.406 g/mL · 1.406 g/mL at 25 °C(lit.)
- Brechungsindex
- 20 · n20/D 1.471(lit.)
- Flammpunkt
- 25 °F · −25 °F
- storage temp.
- -20 °C · -20°C
- Löslichkeit
- reacts
- Aggregatzustand
- Liquid
- Wichte
- 1.47 · 1.47
- Farbe
- Clear colorless to reddish
- Wasserlöslichkeit
- reacts
- BRN
- 1731136 · 1731136
- Stabilität
- Moisture Sensitive (Reactive)
- InChI
- 1S/C3H9ISi/c1-5(2,3)4/h1-3H3
- InChIKey
- CSRZQMIRAZTJOY-UHFFFAOYSA-N
- SMILES
- C[Si](C)(C)I
- CAS Datenbank
- 16029 · 16029-98-4(CAS DataBase Reference)
- NIST chemische Informationen
- Iodotrimethylsilane(16029-98-4)
- EPA chemische Informationen
- Silane, iodotrimethyl- (16029-98-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H225 (98.4%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P303+P361+P353, P304+P340, P305+P354+P338, P316, P317, P321, P363, P370+P378, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 62 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: Silane, iodotrimethyl-
Status: Active Update: 23-11-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/24465
Iodotrimethylsilane: Does not have an individual approval but may be used under an appropriate group standard
Toxikologische Informationen
Sicherheitsdaten
- F
- 8-21
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 2924 3/PG 2
- hs_code
- 29310095
- risk_code
- 11-14-34
- hazard_code
- F,C
- safety_code
- 16-26-36/37/39-43-45-25
- hazard_class
- 3
- packing_group
- II
- Speicherklasse
- 3 - Flammable liquids
- Hazard Classifications
- Eye Dam. 1Flam. Liq. 2Skin Corr. 1B
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
VerwendenIodotrimethylsilane is used for the introduction of trimethylsilyl group in organic synthesis. It is also useful for gas chromatography analysis by converting alcohol into a silyl ether derivative, thereby making it more volatile than the original molecule.Iodotrimethylsilane is a highly efficient reagent for the cleavage of ethers, esters, carbamates, ketals, and lactones. It is also used for the introduction of TMS groups, such as TMS enol ethers, and is a key reagent for the selective removal of N-Cbz groups in the presence of a trimethyltin moiety.This reagent has recently been reported to convert allyl and benzyl phosphotriesters to the corresponding iodides.
Darstellung
synthetischeIodotrimethylsilane is prepared by mixing equimolar amounts of chlorotrimethylsilane and sodium iodide in acetonitrile, reduces various benzylic alcohols to the corresponding phenylalkanes. Other have been reported for the preparation of Trimethylsilyl Iodide(TMS-I): chlorotrimethylsilane undergoes halogen exchange with either lithium iodide in CHCl3 or sodium iodide in MeCN, which allows in situ reagent formation. Alternatively, hexamethyldisilane reacts with iodine at 25–61°C to afford TMS-I with no byproducts.
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