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2,2-dimethyl-1-(methylsulfanyl)propane, also known as tert-butyl methyl sulfide, is an organic compound with the chemical formula C5H12S. It is a colorless, flammable liquid with a distinctive, garlic-like odor. 2,2-dimethyl-1-(methylsulfanyl)propane is a member of the alkyl sulfide family and is characterized by its two methyl groups attached to the central carbon atom, which is also bonded to a methylsulfanyl group. It is used in the synthesis of various organic compounds and as a reagent in chemical reactions. Due to its pungent smell, it is also used as a flavoring agent in the food industry. The compound is relatively stable but can react with strong oxidizing agents and bases. It is important to handle this chemical with care, as it can cause irritation to the eyes, skin, and respiratory system.

6079-57-8

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6079-57-8 Usage

Physical state

Colorless liquid

Odor

Strong

Flammability

Flammable

Boiling point

35°C

Volatility

Highly volatile

Uses

Flavoring agent in the food industry, production of pharmaceuticals, solvent in organic synthesis

Production method

Reaction of isobutene with hydrogen sulfide

Safety precautions

Handle with caution, can cause irritation to eyes and skin

Check Digit Verification of cas no

The CAS Registry Mumber 6079-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6079-57:
(6*6)+(5*0)+(4*7)+(3*9)+(2*5)+(1*7)=108
108 % 10 = 8
So 6079-57-8 is a valid CAS Registry Number.

6079-57-8Downstream Products

6079-57-8Relevant academic research and scientific papers

Gas-Phase Nucleophilic Displacement Reactions

Olmstead, William N.,Brauman, John I.

, p. 1653 - 1662 (2007/10/03)

Displacement reactions of each of a variety of anionic nucleophiles reacting with each of a variety of neutrals have been studied by pulsed ion cyclotron resonance (ICR) spectroscopy.Rate constants for these reactions are interpreted in terms of a three-step reaction sequence.RRKM calculations are used to obtain information about the energy of transition states.The origin of the barrier to reaction in solution is discussed.

Characterization of Monomeric Thiopivaldehyde

Vedejs, Edwin,Perry, David A.,Wilde, Richard G.

, p. 2985 - 2989 (2007/10/02)

The title compound is the first aliphatic thioaldehyde to be observed under odinary laboratory conditions.Its spectral data and chemical characterization are described, including 2+3 cycloadditions with nitronate ester 6, 2+4 cycloaddition with reactive dienes, thiophilic addition with phenyllithium, carbophilic addition with butyllithium, conversion to episulfide 15 by the Wittig reagent, and oxidation to sulfine 17 with MCPBA.Independent generation of thiopivaldehyde from tert-butyllithium + ethyl thionoformate followed by heating 9 in xylene or by cycloreversion of 2-tert-butyl-1,2-dithiolane with butyllithium are also described.

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