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Methanethiol, also known as thiobis-, is a chemical compound with the formula CH3SH. It is a colorless, flammable, and toxic gas with a strong odor of rotten cabbage or sewage. Methanethiol is an organosulfur compound, which means it contains carbon and sulfur atoms bonded together. It is used in various applications, including as a chemical intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it serves as a flavoring agent in the food industry to impart a sulfurous taste to certain products. Methanethiol is also a natural byproduct of the decomposition of certain proteins and is released by some microorganisms, contributing to the smell of certain environments like swamps and sewage treatment plants.

7529-06-8

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7529-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7529-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7529-06:
(6*7)+(5*5)+(4*2)+(3*9)+(2*0)+(1*6)=108
108 % 10 = 8
So 7529-06-8 is a valid CAS Registry Number.

7529-06-8Relevant academic research and scientific papers

NEUE ERGEBNISSE BEI DER SPALTUNG VON THIOETHERN MIT NATRIUM IN FLUESSIGEM AMMONIAK. ABTRENNUNG VON 1.3.5-TRITHIAPENTAN UEBER 1.5-BIS-(TRIMETHYLSILYL)-1.3.5-TRITHIAPENTAN ALS ZWISCHENSTUFE

Weissflog, Eckhard

, p. 233 - 240 (2007/10/02)

Recent results show that the cleavage of oligomeric and polymeric thioformaldehydes or polymethylenedisulfide by sodium in liquid ammonia, followed by treatment with an excess of hydrochloric acid, leads to the formation of mercaptothioethers, CH3(SCH2)nSH, bis-mercaptothioethers, HS(CH2S)mH and thioalkanes, CH3(SCH2)xSCH3.The identification and isolation of various components of these mixtures are described.The separation of pure 1.3.5-trithiapentane by silylation, distillation and cleavage with hydrogen chloride is of interest for its synthesis starting from easily available compounds like s-trithiane, polymethylenesulfide or polymethylenedisulfide.The silylated derivatives of 1.3.5-trithiahexane and 1.3.5-trithiapentane are described.

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