Iodotrimethylsilan

Trimethylsilyl iodide

HCID 85247CAS 16029-98-4

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

Iodotrimethylsilane16029-98-4TrimethyliodosilaneTrimethylsilyl iodideiodo(trimethyl)silaneSilane, iodotrimethyl-7A65KRZ6NVMe3SiIDTXSID4065997TMSI cpdRefChem:148569DTXCID5035161
Weitere Namen anzeigen
TMS iodideCT3610IodotrimethyLTrimethylsilyl ioIodotrmethylsilanetrimethyiodosilaneCo-Formula CFS-710
240-171-0TMSIMFCD00001028Iodotrimethylsilane (>90%)TMISIodotrimethylsilane; TMSI;Trimethylsilicon iodide; Trimethylsilyl iodidetrimethylsilyliodideC3H9ISi

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

Experimentelle und physikochemische Eigenschaften

Chemical ClassesMetals -> Metalloid Compounds (Silicon)
SpringerMaterials Properties29Si nuclear magnetic resonance spectrum
Physical DescriptionClear light brown liquid; [Sigma-Aldrich MSDS]

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

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

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 · 3 Einträge

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

Hazards SummaryReacts violently with water; Causes burns; Inhalation may cause corrosive injuries to upper respiratory tract and lungs; [Sigma-Aldrich MSDS] See Silicon tetraiodide.
Hazard Classes and CategoriesFlam. Liq. 2 (98.4%)

Toxikologische Informationen

Adverse EffectsDermatotoxin - Skin burns.

Sicherheitsdaten

F
8-21
wgk
3
tsca
TSCA listed
ridadr
UN 2924 3/PG 2
hs_code
29310095
risk_code
11-14-34

Chemie und Industrie

Verwendung und Herstellung

UsesUsed as an intermediate; [ExPub: ECHA REACH Registrations]
General Manufacturing InformationSilane, iodotrimethyl-: ACTIVE
Anwendungen · 1 Eintrag

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 · 1 Eintrag

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.

Anbieter50 Anbieter

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