17882-12-1 Usage
Uses
Used in Organic Synthesis:
P-(TRIMETHYLSILYL)BENZENETHIOL is used as a reagent for facilitating selective reactions in organic synthesis. The trimethylsilyl group's protective role allows chemists to target specific functional groups within a molecule, enhancing the efficiency and precision of the synthesis process.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, P-(TRIMETHYLSILYL)BENZENETHIOL is utilized as a key intermediate in the synthesis of various drugs. Its unique structure and reactivity contribute to the development of new and innovative pharmaceutical compounds.
Used in Agrochemical Synthesis:
P-(TRIMETHYLSILYL)BENZENETHIOL also finds application in the agrochemical sector, where it serves as a crucial component in the synthesis of different agrochemicals. Its role in creating specific chemical structures is vital for the development of effective products in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 17882-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,8 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17882-12:
(7*1)+(6*7)+(5*8)+(4*8)+(3*2)+(2*1)+(1*2)=131
131 % 10 = 1
So 17882-12-1 is a valid CAS Registry Number.
17882-12-1Relevant academic research and scientific papers
Development of Odorless Thiols and Sulfides and Their Applications to Organic Synthesis
Nishide, Kiyoharu,Ohsugi, Shin-Ichi,Miyamoto, Tetsuo,Kumar, Kamal,Node, Manabu
, p. 189 - 200 (2007/10/03)
Development of new odorless thiols (dodecanethiol, 4-n- heptylphenylmethanethiol, 4-trimethylsilylphenylmethanethiol, 4-trimethylsilylbenzenethiol) and an odorless sulfide (1-methylsulfanyldodecane) and their applications to dealkylation, Michael addition, Swern oxidation, and Corey-Kim oxidation are described.
Synthetic equivalents of benzenethiol and benzyl mercaptan having faint smell: Odor reducing effect of trialkylsilyl group
Nishide, Kiyoharu,Miyamoto, Tetsuo,Kumar, Kamal,Ohsugi, Shin-Ichi,Node, Manabu
, p. 8569 - 8573 (2007/10/03)
Syntheses and odor tests of the trialkylsilylated benzyl mercaptans and benzenethiols have revealed that the trimethylsilyl substituent on the benzene ring has a remarkable effect in reducing the foul smell of the parent benzyl mercaptan and benzenethiol.
