CAS 16911-89-0
:phenyl chlorodithioformate
Description:
Phenyl chlorodithioformate is an organosulfur compound characterized by its unique functional groups, specifically the dithioester moiety. It typically appears as a colorless to pale yellow liquid with a pungent odor. This compound is known for its reactivity, particularly in nucleophilic substitution reactions, where it can act as a sulfur donor. Its structure features a phenyl group attached to a chlorodithioformate functional group, which contributes to its chemical properties and reactivity. Phenyl chlorodithioformate is often used in organic synthesis, particularly in the preparation of thioesters and as a reagent in various chemical transformations. Due to its sulfur content, it can also exhibit properties such as being a potential source of thiol groups in reactions. Safety precautions are necessary when handling this compound, as it can be toxic and irritating to the skin and respiratory system. Proper storage and handling protocols should be followed to mitigate any risks associated with its use.
Formula:C7H5ClS2
InChI:InChI=1/C7H5ClS2/c8-7(9)10-6-4-2-1-3-5-6/h1-5H
SMILES:c1ccc(cc1)SC(=S)Cl
Synonyms:- Phenyl Carbonochloridodithioate
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Found 3 products.
Phenyl Chlorodithioformate
CAS:Formula:C7H5ClS2Purity:>97.0%(GC)Color and Shape:Light yellow to Amber to Dark green clear liquidMolecular weight:188.69Carbonochloridodithioic acid, phenyl ester
CAS:Formula:C7H5ClS2Purity:97%Color and Shape:LiquidMolecular weight:188.6976Phenyl carbonochloridodithioate
CAS:Formula:C7H5ClS2Purity:95.0%Color and Shape:Liquid, ClearMolecular weight:188.69


