Methyl Dimethyldithiocarbamate
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Methyl Dimethyldithiocarbamate
Methyl dimethyldithiocarbamate is the organosulfur compound with the formula (CH3)2NC(S)SCH3. It is the one of simplest dithiocarbamic esters. It is a white volatile solid that is poorly soluble in water but soluble in many organic solvents. It was once used as a pesticide. Methyl dimethyldithiocarbamate can be prepared by methylation of salts of dimethyldithiocarbamate: :(CH3)2NCS2Na + (CH3O)2SO2 → (CH3)2NC(S)SCH3 + Na H3OSO3 It can also be prepared by the reaction of a tetramethylthiuram disulfide Thiuram disulfides are a class of organosulfur compounds with the formula (R2NCSS)2. Many examples are known, but popular ones include R = Me and Et. They are disulfides obtained by oxidation of the dithiocarbamates. These compounds are used i ... with methyl Grignard reagents:{{cite journal, title=Reaction of Grignard Reagents with Tetramethylthiuram Disulfide ielding dithiocarbamatesauthor=John R. Grunwell, journal=J. Org. Chem., year=1970, volume=35, issue=5, pa ...
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Organosulfur Compound
Organosulfur compounds are organic compounds that contain sulfur. They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin. Nature abounds with organosulfur compounds—sulfur is vital for life. Of the 20 common amino acids, two ( cysteine and methionine) are organosulfur compounds, and the antibiotics penicillin and sulfa drugs both contain sulfur. While sulfur-containing antibiotics save many lives, sulfur mustard is a deadly chemical warfare agent. Fossil fuels, coal, petroleum, and natural gas, which are derived from ancient organisms, necessarily contain organosulfur compounds, the removal of which is a major focus of oil refineries. Sulfur shares the chalcogen group with oxygen, selenium, and tellurium, and it is expected that organosulfur compounds have similarities with carbon–oxygen, carbon–selenium, and carbon–tellurium compounds. A classical chemical test for the detection of sulfur co ...
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Methylation
In the chemical sciences, methylation denotes the addition of a methyl group on a substrate, or the substitution of an atom (or group) by a methyl group. Methylation is a form of alkylation, with a methyl group replacing a hydrogen atom. These terms are commonly used in chemistry, biochemistry, soil science, and the biological sciences. In biological systems, methylation is catalyzed by enzymes; such methylation can be involved in modification of heavy metals, regulation of gene expression, regulation of protein function, and RNA processing. In vitro methylation of tissue samples is also one method for reducing certain histological staining artifacts. The reverse of methylation is demethylation. In biology In biological systems, methylation is accomplished by enzymes. Methylation can modify heavy metals, regulate gene expression, RNA processing and protein function. It has been recognized as a key process underlying epigenetics. Methanogenesis Methanogenesis, the process th ...
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Thiuram Disulfide
Thiuram disulfides are a class of organosulfur compounds with the formula (R2NCSS)2. Many examples are known, but popular ones include R = Me and Et. They are disulfides obtained by oxidation of the dithiocarbamates. These compounds are used in sulfur vulcanization of rubber as well as pesticides and drugs. They are typically white or pale yellow solids that are soluble in organic solvents. Preparation, structure, reactions They are prepared by the oxidation of the salts of the corresponding dithiocarbamates (e.g. sodium diethyldithiocarbamate). Typical oxidants are chlorine and hydrogen peroxide: :2 R2NCSSNa + Cl2 → (R2NCSS)2 + 2 NaCl Thiuram disulfides react with Grignard reagents to give esters of dithiocarbamic acid, as in the preparation of methyl dimethyldithiocarbamate: : e2NC(S)Ssub>2 + MeMgX → Me2NC(S)SMe + Me2NCS2MgX The compounds feature planar dithiocarbamate subunits and are linked by an S−S bond of 2.00  Å. The C(S)−N bond is sh ...
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