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S-2-(phenylcarbamoyl)phenyl benzothioate is a complex organic chemical compound with the molecular formula C19H15NO2S. It is a derivative of benzothioate, featuring a phenylcarbamoyl group attached to the 2-position of the benzene ring. S-2-(phenylcarbamoyl)phenyl benzothioate is characterized by its aromatic structure, with two phenyl rings connected through a benzothioate linkage. The phenylcarbamoyl group adds a urea-like functionality to the molecule, which can influence its reactivity and properties. S-2-(phenylcarbamoyl)phenyl benzothioate may be of interest in chemical research and pharmaceutical development due to its unique structure and potential applications in the synthesis of more complex molecules or as a precursor in organic synthesis.

1677-26-5

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1677-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1677-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1677-26:
(6*1)+(5*6)+(4*7)+(3*7)+(2*2)+(1*6)=95
95 % 10 = 5
So 1677-26-5 is a valid CAS Registry Number.

1677-26-5Downstream Products

1677-26-5Relevant academic research and scientific papers

A new paradigm for carbon-carbon bond formation: Aerobic, copper-templated cross-coupling

Villalobos, Janette M.,Srogl, Jiri,Liebeskind, Lanny S.

, p. 15734 - 15735 (2008/09/20)

Thiol esters and boronic acids react to produce ketones under aerobic conditions in the presence of catalytic quantities of a CuI or CuII salt. The reaction occurs at reasonable rates between room temperature and 50 °C at neutral pH using thiol esters derived from bulky 2° amides of thiosalicylamides such as those based on N-tert-butyl-2-mercaptobenzamide. In this mechanistically unprecedented reaction system, the carbon-carbon bond formation occurs through templating of the thiol ester and the boronic acid at copper; the system is rendered catalytic in copper under the aerobic conditions. Copyright

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