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Trimethyl-(3-phenylsulfanyl-propoxy)-silane is an organosilicon compound with the chemical formula C12H21OSSi. It is a colorless liquid at room temperature and is soluble in organic solvents. Trimethyl-(3-phenylsulfanyl-propoxy)-silane is characterized by a silicon atom bonded to three methyl groups and a propoxy group, which is further connected to a phenylsulfanyl group. The phenylsulfanyl group consists of a sulfur atom bonded to a benzene ring, providing the molecule with unique properties. It is used in various applications, including as a coupling agent in the synthesis of organic-inorganic hybrid materials and as a reagent in the formation of silyl ethers. Due to its reactivity, it is important to handle Trimethyl-(3-phenylsulfanyl-propoxy)-silane with care, typically in a controlled environment and with appropriate safety measures.

20486-07-1

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20486-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20486-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,8 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20486-07:
(7*2)+(6*0)+(5*4)+(4*8)+(3*6)+(2*0)+(1*7)=91
91 % 10 = 1
So 20486-07-1 is a valid CAS Registry Number.

20486-07-1Relevant academic research and scientific papers

O-SILYLATED ENOLATE PHENYLTHIOALKYLATION: a SYNTHESIS OF α,β-UNSATURATED 5- AND 6-MEMBERED LACTONES.

Khan, Hassan A.,Paterson, Ian

, p. 5083 - 5084 (2007/10/02)

ZnBr2-catalysed phenylthioalkylation of keten bis(trimethylsilyl)acetals, obtained from carboxylic acids, with appropriate α-chlorosulphides can be used to prepare γ- and δ-lactones.

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