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33577-16-1

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33577-16-1 Usage

Chemical Properties

Clear colorless to yellow liquid

Uses

(Methylthio)dimethyl sulfoxide is a essential oil from fruit of Gallesia integrifolia exhibit antifungal activity against Aspergillus fumigatus, Aspergillus niger and Aspergillus ochraceus.

Check Digit Verification of cas no

The CAS Registry Mumber 33577-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,7 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33577-16:
(7*3)+(6*3)+(5*5)+(4*7)+(3*7)+(2*1)+(1*6)=121
121 % 10 = 1
So 33577-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H8OS2/c1-5-3-6(2)4/h3H2,1-2H3/t6-/m0/s1

33577-16-1 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (M0805)  Methyl (Methylsulfinyl)methyl Sulfide  >96.0%(GC)

  • 33577-16-1

  • 5g

  • 390.00CNY

  • Detail
  • TCI America

  • (M0805)  Methyl (Methylsulfinyl)methyl Sulfide  >96.0%(GC)

  • 33577-16-1

  • 25g

  • 1,210.00CNY

  • Detail
  • Alfa Aesar

  • (L00510)  Methyl (methylthio)methyl sulfoxide, 97%   

  • 33577-16-1

  • 10g

  • 553.0CNY

  • Detail

33577-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methylsulfanyl(methylsulfinyl)methane

1.2 Other means of identification

Product number -
Other names methanesulfinyl-methylsulfanyl-methane

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:33577-16-1 SDS

33577-16-1Relevant articles and documents

Ogura,Tsuchihashi

, p. 1689 (1970)

Oxidation of Dithia Compounds: Comparative Experimental and Theoretical Studies on 1,3-Bis(methylthio)propane, Bis(methylthio)methane, and meso-4,6-Dimethyl-1,3-dithiane

González, Victorino Vallejos,Podlech, Joachim

, p. 5430 - 5442 (2021/10/25)

1,3-Bis(methylthio)propane, bis(methylthio)methane, and meso-4,6-dimethyl-1,3-dithiane were oxidized with 1–4 equivalents of hydrogen peroxide, meta-chloroperbenzoic acid, sodium periodate, or potassium permanganate, respectively, and the amounts of oxidized substrates (sulfoxides and/or sulfones) were determined by NMR spectroscopy. Sulfanyl groups in the former starting material turned out to behave like independent functions, while a mutual influence of the sulfur functions was verified in the latter compounds. A meaningful investigation was possible in the conformationally constrained dithiane derivative. Oxidation of the dithiane with stoichiometric amounts of periodate led to exclusive formation of bissulfoxides, while hydrogen peroxide and meta-chloroperbenzoic acid yielded the possible products less specifically and permanganate preferentially furnished sulfones. The experimental investigations were supported by calculations on energies and stereoelectronic effects of starting materials, products, and transition states. The unique property of permanganate to exclusively yield sulfones might be due to its special oxidation mechanism, where the sulfur is not only acting as nucleophile, but concomitantly as electrophilic moiety.

Selective oxidation of sulfides to sulfoxides by a molybdate-based catalyst using 30% hydrogen peroxide

Bayat, Ahmad,Shakourian-Fard, Mehdi,Hashemi, Mohammad Mahmoodi

, p. 16 - 21 (2014/05/20)

An efficient method is reported for selective oxidation of various types of sulfides to sulfoxides and sulfones in good to high yields using 30% H 2O2 in the presence of catalytic amounts of molybdate-based catalyst in acetonitrile as solvent at room temperature. The catalyst can be easily recovered and reused for seven reaction cycles without considerable loss of activity.

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