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1-oxo-2-phenyl-3-indenethiol is an organic compound with the molecular formula C15H11OS. It is a derivative of indan-1-one, featuring a phenyl group at the 2-position and a thiol group at the 3-position. This chemical is characterized by its unique structure, which includes a five-membered ring fused to a six-membered aromatic ring, with the thiol group attached to the carbon adjacent to the carbonyl group. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound is also known for its distinct odor, which can be described as a combination of sulfur and aromatic characteristics.

52711-19-0

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52711-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52711-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,1 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52711-19:
(7*5)+(6*2)+(5*7)+(4*1)+(3*1)+(2*1)+(1*9)=100
100 % 10 = 0
So 52711-19-0 is a valid CAS Registry Number.

52711-19-0Downstream Products

52711-19-0Relevant academic research and scientific papers

Hydrothiolysis of carbofunctional α,β-unsaturated sulfides as an approach to the synthesis of 1,7-dithiocarbonyl compounds

Timokhina,Sokol'nikova,Kanitskaya,Yashchenko,Toryashinova,Voronkov

, p. 1208 - 1212 (2007/10/03)

Bis(1-N,N-dimethylimmonio-3-phenylprop-2-en-3-yl) sulfide diperchlorate and (1-N,N-dimethyl-immonio-3-phenylprop-2-en-3-yl) (5,5-dimethyl-1- morpholiniocyclohex-2-en-3-yl) sulfide diperchlorate react with hydrogen sulfide giving rise to the corresponding

α,β-UNSATURATED THIO COMPOUNDS. SYNTHESIS AND SOME CHEMICAL TRANSFORMATIONS OF THE THIO DERIVATIVES OF 2-ARYL-1-INDANONES AND 2-ARYL-1,3-INDANEDIONES

Petriashvili, K. A.,Usov, V. A.,Voronkov, M. G.

, p. 507 - 512 (2007/10/02)

In the reaction of 2-aryl-1-indanones and 2-aryl-1,3-indanediones with hydrogen sulfide in the presence of hydrogen chloride 2-aryl-3-indenethiols and 3-mercapto-2-aryl-1-indenethiones respectively are formed.The latter are readily acylated, condense with

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