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DIMETHYL(METHYLTHIO)SULFONIUM TETRAFLUOROBORATE is a chemical compound belonging to the sulfonium class of organic compounds, characterized by the molecular formula (CH3)2S+(CH3S)BF4-. It is a white to off-white solid with a melting point of approximately 100-105°C. DIMETHYL(METHYLTHIO)SULFONIUM TETRAFLUOROBORATE is soluble in polar solvents like methanol and acetonitrile, but not in non-polar solvents such as hexane. It is widely recognized for its role as a mild and selective methylating agent in various organic synthesis processes.

5799-67-7

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5799-67-7 Usage

Uses

Used in Organic Synthesis:
DIMETHYL(METHYLTHIO)SULFONIUM TETRAFLUOROBORATE is used as a mild and selective methylating agent for the alkylation of various substrates in organic synthesis. Its application is particularly valuable due to its ability to selectively introduce methyl groups without causing unwanted side reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIMETHYL(METHYLTHIO)SULFONIUM TETRAFLUOROBORATE is utilized as a reagent in the methylation of nitrogen-containing compounds. This process is crucial for the synthesis of various pharmaceutical compounds, where the introduction of a methyl group can significantly alter the biological activity and properties of the target molecule.
Used in Chemical Research:
DIMETHYL(METHYLTHIO)SULFONIUM TETRAFLUOROBORATE is also employed in chemical research for the study of reaction mechanisms and the development of new synthetic methodologies. Its selective methylating properties make it a valuable tool for exploring the reactivity of different functional groups and designing novel chemical reactions.
Overall, DIMETHYL(METHYLTHIO)SULFONIUM TETRAFLUOROBORATE is a versatile chemical compound with a wide range of applications in organic synthesis, pharmaceuticals, and chemical research, primarily due to its selective methylating capabilities and compatibility with various substrates.

Check Digit Verification of cas no

The CAS Registry Mumber 5799-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5799-67:
(6*5)+(5*7)+(4*9)+(3*9)+(2*6)+(1*7)=147
147 % 10 = 7
So 5799-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H15F3N2O3/c1-3-10-8-13(21,14(15,16)17)19(18-10)12(20)9-4-6-11(22-2)7-5-9/h4-7,21H,3,8H2,1-2H3

5799-67-7 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • TCI America

  • (D1945)  Dimethyl(methylthio)sulfonium Tetrafluoroborate  >97.0%(T)

  • 5799-67-7

  • 1g

  • 1,100.00CNY

  • Detail
  • TCI America

  • (D1945)  Dimethyl(methylthio)sulfonium Tetrafluoroborate  >97.0%(T)

  • 5799-67-7

  • 5g

  • 3,850.00CNY

  • Detail
  • Aldrich

  • (294063)  Dimethyl(methylthio)sulfoniumtetrafluoroborate  97%

  • 5799-67-7

  • 294063-1G

  • 1,074.06CNY

  • Detail

5799-67-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl(methylsulfanyl)sulfanium,tetrafluoroborate

1.2 Other means of identification

Product number -
Other names dimethyl(methylthio)sulfonium tetrafluoroborate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5799-67-7 SDS

5799-67-7Relevant academic research and scientific papers

The oxidation of dimethyl sulphide, trimethylamine, and trimethylphosphine by solvated copper(II) or thallium(III) hexafluorometallates in acetonitrile

Siddique, Rana M.,Winfield, John M.

, p. 1780 - 1784 (2007/10/02)

Dimethyl sulphide, trimethylamine, and trimethylphosphine are oxidized by solvated copper(II) hexafluorophosphate or solvated thallium(III) hexafluorouranate(V) in acetonitrile at room temperature.The reactions are all very similar and spectroscopic studies suggest that the oxidized products are the dinuclear, non-metal cations+, +, and 2+.The compound 2 is obtained from the oxidation of PMe3 by diiodine in MeCN, followed by treatment with nitrosonium hexafluorophosphate.Coloured intermediates observed in the reactions of solvated CuII are formulated as redox-active cations x(NCMe)y>2+, L = SMe2, NMe3, or PMe3, and a generalized reaction scheme is proposed.Key words: copper(II), thallium(III), acetonitrile, oxidation, fluorometallate

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