57903
(Iodomethyl)trimethylsilane
≥99.0% (GC)
Synonym(s):
(Trimethylsilyl)methyl iodide
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About This Item
Linear Formula:
(CH3)3SiCH2I
CAS Number:
Molecular Weight:
214.12
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-123-6
Beilstein/REAXYS Number:
1731485
MDL number:
Quality Level
assay
≥99.0% (GC)
refractive index
n20/D 1.491
bp
139-141 °C (lit.)
density
1.443 g/mL at 25 °C (lit.)
functional group
iodo
SMILES string
C[Si](C)(C)CI
InChI
1S/C4H11ISi/c1-6(2,3)4-5/h4H2,1-3H3
InChI key
VZNYXGQMDSRJAL-UHFFFAOYSA-N
Other Notes
Starting material for the preparation of 2-(trimethylsilyl)ethyl-triphenylphosphonium iodide used for the synthesis of allyl silanes; Used for the N-alkylation of amides, in a reaction sequence to prepare unstabilized ylides for [2+3]-cycloadditions
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
84.2 °F - closed cup
flash_point_c
29 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Articles
Review SET mechanism in photoredox catalysis for sustainable reactions and rearrangement of oxaziridines.
E. Vedejs et al.
The Journal of Organic Chemistry, 48, 4773-4773 (1983)
D. Seyferth et al.
The Journal of Organic Chemistry, 42, 3104-3104 (1977)
I. Fleming et al.
Synthesis, 446-446 (1979)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| O0225000 | 04061833836750 |
| Y0000543 | 04061833795613 |
| Y0000543-0.008MG | 04061832621432 |
| O-902-1ML | 04061834212430 |
| O0225000-50MG | 04061832621401 |
| O5254-50MG | 04061834233985 |
| 57903-5ML | 04061837912382 |
| 57903-25ML | 04061832629551 |