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Bis(m-methylphenylthio)methane, also known as 1,3-bis(3-methylphenylthio)propane, is an organic compound with the chemical formula C15H18S2. It is a colorless to pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. bis(m-methylphenylthio)methane is characterized by its two m-methylphenylthio groups attached to a propane chain, which gives it unique chemical properties. It is used as a ligand in coordination chemistry, particularly in the formation of metal complexes, and has applications in the synthesis of various organometallic compounds. Due to its stability and reactivity, bis(m-methylphenylthio)methane is a valuable building block in the development of new materials and catalysts.

2393-95-5

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2393-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2393-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2393-95:
(6*2)+(5*3)+(4*9)+(3*3)+(2*9)+(1*5)=95
95 % 10 = 5
So 2393-95-5 is a valid CAS Registry Number.

2393-95-5Downstream Products

2393-95-5Relevant academic research and scientific papers

Reduction of CO2 into Methylene Coupled with the Formation of C-S Bonds under NaBH4/I2 System

Guo, Zhiqiang,Zhang, Bo,Wei, Xuehong,Xi, Chanjuan

supporting information, p. 6678 - 6681 (2018/10/24)

A selective four-electron reduction of CO2 with thiophenol using NaBH4 as a reductant is described to access dithioacetals. This reaction provides a novel synthetic method for the highly selective conversion of CO2 into methylene, and a new access to molecular structures via formation of C-S bonds using CO2 as the C1 source.

Cs2CO3-promoted methylene insertion into disulfide bonds using acetone as a methylene source

Chen, Qian,Yu, Guodian,Wang, Xiaofeng,Huang, Yulin,Yan, Yan,Huo, Yanping

supporting information, p. 4086 - 4089 (2018/06/12)

An efficient halogen-free Cs2CO3-promoted methylene insertion into disulfide bonds has been achieved using acetone as a methylene source under mild conditions. This method provides a convenient and practical route to dithioacetals in up to 96% yield with good functional group compatibility.

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