CAS 201611-77-0

Benzenecarbodithioic acid, 1-methyl-1-phenylethyl ester

Description:

Benzenecarbodithioic acid, 1-methyl-1-phenylethyl ester, identified by its CAS number 201611-77-0, is an organic compound characterized by the presence of a dithioic acid functional group and an ester linkage. This compound typically exhibits a yellow to brown color and is soluble in organic solvents, reflecting its non-polar characteristics. The presence of the methyl and phenyl groups contributes to its hydrophobic nature and may influence its reactivity and interaction with other chemical species. As a dithioic acid derivative, it may participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. Its applications could span across fields such as organic synthesis, materials science, and potentially in the development of agrochemicals or pharmaceuticals, although specific applications may vary based on its reactivity and stability. Safety data should be consulted for handling and storage, as compounds with similar structures can exhibit toxicity or environmental hazards.

Formula: C₁₆H₁₆S₂

2-Phenylpropan-2-yl Benzodithioate

CAS: 201611-77-0

Formula: C₁₆H₁₆S₂

Purity: >98.0%(HPLC)

Color and Shape: Red to Dark red to Dark purple powder to lump to clear liquid

Molecular weight: 272.42

Ref: 3B-P2638

2-Phenyl-2-propylbenzodithiolate, min. 97%

CAS: 201611-77-0

2-Phenyl-2-propylbenzodithiolate, min. 97%

Formula: C₁₆H₁₆S₂

Purity: min. 97%

Color and Shape: dark red-purple liq.

Molecular weight: 272.43

Ref: 08-16-0513

Benzenecarbodithioic acid, 1-methyl-1-phenylethyl ester

CAS: 201611-77-0

Formula: C₁₆H₁₆S₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 272.4282

Ref: IN-DA002DJY

2-Phenylpropan-2-yl benzodithioate

CAS: 201611-77-0

2-Phenylpropan-2-yl benzodithioate

Purity: 99%

Molecular weight: 272.43g/mol

Ref: 54-OR94184

2-Phenyl-2-propylbenzodithiolate

CAS: 201611-77-0

2-Phenyl-2-propylbenzodithiolate is a reactive chemical with a number of industrial uses, including as a dye in the textile industry and as a fluorescence probe. 2-Phenyl-2-propylbenzodithiolate binds to metal ions and forms stable complexes that are not easily hydrolyzed. It has been used to detect the presence of zinc ions in cell culture media using FTIR spectroscopy. The product can also be used for synchronous fluorescence measurements, which can be used for kinetic studies. 2-Phenyl-2-propylbenzodithiolate is synthesized by the reaction of phenylmercury dibromide with 2-(2'-chlorophenoxy)ethyl acetate in an organic solvent such as cyclohexane.

Formula: C₁₆H₁₆S₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 272.43 g/mol

Ref: 3D-BIA61177

2-Phenylpropan-2-yl benzodithioate

CAS: 201611-77-0

Formula: C₁₆H₁₆S₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 272.42

Ref: 10-F540344