Home Iodos 2181-42-2
2181-42-2,MFCD00011632
Catalog No.:AA003V1U

2181-42-2 | Trimethylsulfonium iodide

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5g
98%
in stock  
$7.00   $5.00
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10g
98%
in stock  
$10.00   $7.00
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25g
98%
in stock  
$20.00   $14.00
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100g
95%
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$72.00   $50.00
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500g
98%
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$178.00   $125.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003V1U
Chemical Name:
Trimethylsulfonium iodide
CAS Number:
2181-42-2
Molecular Formula:
C3H9IS
Molecular Weight:
204.0730
MDL Number:
MFCD00011632
SMILES:
C[S+](C)C.[I-]
NSC Number:
36713
Properties
Properties
 
Form:
Solid  
MP:
215-220 °C(lit.)  
Solubility:
400g/l  
Stability:
Light Sensitive  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
8  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
1  

Downstream Synthesis Route

[1]CanadianJournalofChemistry,1969,vol.47,p.4327-4333

4903-09-7    2181-42-2   
2-(3-chloro-4-methoxyphenyl)oxirane 

[1]BioorganicandMedicinalChemistry,2017,vol.25,p.293-304

[2]JournalofMedicinalChemistry,1982,vol.25,p.352-358

13726-16-4    2181-42-2   
2-(4-Chloro-3-methoxy-phenyl)-oxirane 

[1]JournalofMedicinalChemistry,1982,vol.25,p.352-358

[1]Tetrahedron,1988,vol.44,p.81-90

[1]OrganicLetters,2011,vol.13,p.4786-4789

[2]EuropeanJournalofMedicinalChemistry,2018,vol.143,p.21-32

[3]JournalofOrganicChemistry,1981,vol.46,p.3259-3262

[4]Bioorganicandmedicinalchemistry,2020

Literature

Title: Use of an injection port for thermochemolysis-gas chromatography/mass spectrometry: rapid profiling of biomaterials.

Journal: Journal of chromatography. A 20090731

Title: Reaction efficiency of organic alkalis with various classes of lipids during thermally assisted hydrolysis and methylation.

Journal: Journal of chromatography. A 20090410

Title: Urea derivatives are highly active catalysts for the base-mediated generation of terminal epoxides from aldehydes and trimethylsulfonium iodide.

Journal: Organic & biomolecular chemistry 20080421

Title: Study of different parameters affecting the derivatization of acidic herbicides with trimethylsulfonium hydroxide to make them suitable for gas chromatography analysis.

Journal: Journal of chromatography. A 20060901

Title: Trimethylsulfonium hydroxide as derivatization reagent for the chemical investigation of drying oils in works of art by gas chromatography.

Journal: Journal of chromatography. A 20040820

Title: Evaluation of the cholinomimetic actions of trimethylsulfonium, a compound present in the midgut gland of the sea hare Aplysia brasiliana (Gastropoda, Opisthobranchia).

Journal: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 20020401

Title: A mechanistic analysis of penetration of glyphosate salts across astomatous cuticular membranes.

Journal: Pest management science 20020401

Title: Solvent effects on methyl transfer reactions. 2. The reaction of amines with trimethylsulfonium salts.

Journal: Journal of the American Chemical Society 20010627

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