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Benzenethiol, pentakis(methylthio)-, also known as 1,2,3,4,5-pentakis(methylthio)benzene, is an organic compound with the chemical formula C9H12S5. It is a derivative of benzene, where each hydrogen atom on the benzene ring is replaced by a methylthio group (-SCH3). This results in a highly symmetrical molecule with five methylthio substituents attached to the benzene core. The compound is characterized by its strong, pungent odor and is used in various applications, such as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential toxicity, it is essential to handle Benzenethiol, pentakis(methylthio)- with proper safety precautions and in accordance with relevant regulations.

70648-33-8

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70648-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70648-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,4 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70648-33:
(7*7)+(6*0)+(5*6)+(4*4)+(3*8)+(2*3)+(1*3)=128
128 % 10 = 8
So 70648-33-8 is a valid CAS Registry Number.

70648-33-8Downstream Products

70648-33-8Relevant academic research and scientific papers

Reactions of Polychlorobenzenes with Alkanethiol Anions in HMPA. A Simple, High-Yield Synthesis of Poly(alkylthio)benzenes

Testaferri, Lorenzo,Tingoli, Marco,Tiecco, Marcello

, p. 4376 - 4380 (2007/10/02)

Reactions of the isomeric trichlorobenzenes and tetrachlorobenzenes and of pentachloro- and hexachlorobenzene with an excess of the sodium salt of the isopropanethiol, in HMPA, afforded the products of complete displacement of all the chlorine atoms present in the molecule.Similar substitutions were also obtained with EtSNa.The reactions with MeSNa were in some cases complicated by the competitive nucleophilic attack at the methyl group of the initially formed aryl methyl thioethers which are thus demethylated to afford thiophenols.

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