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β-Hydroxy dithiocinnamic methyl ester is a chemical compound with the molecular formula C11H10O2S2. It is a derivative of dithiocinnamic acid, featuring a β-hydroxy group and a methyl ester functional group. This organic compound is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical structure and reactivity. It is characterized by its ability to form chelates with metal ions, which can be useful in the synthesis of complex organic molecules and in the development of new drugs. The compound's properties, such as its solubility and stability, make it a subject of interest for researchers exploring its potential uses and interactions within different chemical systems.

17666-73-8

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17666-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17666-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,6 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17666-73:
(7*1)+(6*7)+(5*6)+(4*6)+(3*6)+(2*7)+(1*3)=138
138 % 10 = 8
So 17666-73-8 is a valid CAS Registry Number.

17666-73-8Relevant academic research and scientific papers

Platinum(ii) O,S complexes as potential metallodrugs against Cisplatin resistance

Hildebrandt, Jana,H?fner, Norman,G?rls, Helmar,Kritsch, Daniel,Ferraro, Giarita,Dürst, Matthias,Runnebaum, Ingo B.,Merlino, Antonello,Weigand, Wolfgang

supporting information, p. 18876 - 18891 (2016/12/09)

We report on platinum(ii) complexes with different cinnamic acid derivatives as ligands with cytotoxic activity against Cisplatin resistant ovarian cancer cell line subcultures of SKOV3 and A2780. A typical mechanism of action for platinum(ii) complexes a

Dimsyl anion induced demethylation and fragmentation reactions of α-oxoketenedithioacetals

Nair,Samuel,Asokan

, p. 573 - 576 (2007/10/03)

Base induced S-demethylation of dimethyl α-oxoketenedithioacetals with dimsyl sodium gave methyl β-oxodithiocarboxylates in good yields while cyclic ketenedithioacetals having a 1,3-dithiolane moiety underwent a fragmentation reaction leading to vinyl β-oxodithiocarboxylates.

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