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线性分子式:
(CH3)3S(I)
化学文摘社编号:
分子量:
204.07
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-555-4
Beilstein/REAXYS Number:
3555192
MDL number:
Assay:
98%
InChI key
VFJYIHQDILEQNR-UHFFFAOYSA-M
InChI
1S/C3H9S.HI/c1-4(2)3;/h1-3H3;1H/q+1;/p-1
SMILES string
[I-].C[S+](C)C
assay
98%
reaction suitability
reaction type: C-C Bond Formation
mp
215-220 °C (lit.)
Quality Level
General description
三甲基磺酸碘通常用作有机合成中的甲基化剂。
Application
用强碱处理可生成二甲基亚甲基锍,而后又可参与酮的羰基原位反应形成环氧化物或烯丙醇。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
H Castejon et al.
Journal of the American Chemical Society, 123(25), 6092-6097 (2001-06-21)
The reaction of ammonia and pyridine with trimethylsulfonium ion has been studied in gas phase and solution. Density functional theory at the B3LYP/6-31+G level was used to describe the energy changes along the reaction coordinate in the gas phase, and
Jörg Schönherr
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Penetration of glyphosate salts across isolated poplar (Populus canescens (Aiton) Sm) cuticular membranes (CM) was studied using Na+, K+, NH4+, trimethylsulfonium+ (TMS) and isopropylamine+ (IPA) as cations. After droplet drying, humidity over the salt residues on the outer surfaces of
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Journal of chromatography. A, 1216(15), 3296-3299 (2009-02-19)
Reaction efficiencies of two organic alkalis, tetramethylammonium hydroxide (TMAH) and trimethylsulfonium hydroxide (TMSH), with lipids during thermally assisted hydrolysis and methylation (THM) were examined focusing on (1) the types of lipids and (2) degree of unsaturation of fatty acid moieties.
Tetrahedron Letters, 35, 2009-2009 (1994)
C Díez et al.
Journal of chromatography. A, 1125(2), 244-253 (2006-06-20)
In this study, an orthogonal array design was applied to know the way different parameters affected the derivatization of some herbicides that are commonly applied in the soils. Herbicides formulated as esters have been reported to rapidly hydrolyse, in contact
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