626-26-6 Usage
Description
DI-SEC-BUTYL SULFIDE is an organic compound with the chemical formula C8H18S. It is a colorless liquid with a strong, unpleasant odor. DI-SEC-BUTYL SULFIDE is known for its unique chemical properties and has been utilized in various applications across different industries.
Uses
Used in Analytical Chemistry:
DI-SEC-BUTYL SULFIDE is used as a chemical reference material for the determination of dialkyl sulfides. It plays a crucial role in the development and validation of novel micropacked columns prepared from the slurry of bis[1,2-bis(4-n-undecyloxyphenyl)ethane-1,2-dithiolene]nickel(II) coated on chromosorb W. This application is particularly relevant in micropacked gas chromatography, where the compound aids in the accurate identification and quantification of dialkyl sulfides in various samples.
Check Digit Verification of cas no
The CAS Registry Mumber 626-26-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 626-26:
(5*6)+(4*2)+(3*6)+(2*2)+(1*6)=66
66 % 10 = 6
So 626-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H18S/c1-5-7(3)9-8(4)6-2/h7-8H,5-6H2,1-4H3
626-26-6Relevant articles and documents
Direct synthesis of disulfides from alkyl halides using thiourea and CCl4 in glycerol
Abbasi, Mohammad,Khalili, Dariush
, p. 1425 - 1430 (2015/06/22)
Abstract Dialkyl disulfides were obtained on the basis of the reaction of alkyl halides and thiourea in the presence of CCl4 and Et3N. This procedure enables the odorless and one-pot synthesis of disulfides by employing cheap, easy-to-handle and readily available reagents and substrates in wet glycerol.
Deoxygenation of sulfoxides with silica chloride
Mohanazadeh, Farajollah,Momeni, Ahmad Reza,Ranjbar, Yousef
, p. 6127 - 6128 (2007/10/02)
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Deoxygenation and Desulphuration Reactions of Lithium: Part V - Reaction of Sulphoxides with Lithium
Rajanikanth, B.,Ravindranath, B.
, p. 296 - 297 (2007/10/02)
Dialkyl and aralkyl sulphoxides are reduced to the corresponding sulphides in good yields by lithium in dimethoxyethane; however, the reaction of benzyl sulphoxides with lithium is more complex.