54576-40-8 Usage
Uses
Used in Fragrance Industry:
1-Methyl-4-(sec-butylthio)benzene is used as a scent ingredient for its aromatic and slightly sweet odor, contributing to the creation of various fragrances.
Used in Food Industry:
In addition to its application in fragrances, 1-Methyl-4-(sec-butylthio)benzene is used as a flavoring agent in food products, enhancing the taste and aroma of certain dishes.
Used in Chemical Industry:
1-Methyl-4-(sec-butylthio)benzene is utilized as a chemical intermediate in the manufacturing of various industrial products, playing a crucial role in the synthesis of different compounds.
Safety Note:
It is important to handle 1-Methyl-4-(sec-butylthio)benzene with caution, as it may pose hazards if not used or stored properly, emphasizing the need for proper safety measures during its application in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 54576-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54576-40:
(7*5)+(6*4)+(5*5)+(4*7)+(3*6)+(2*4)+(1*0)=138
138 % 10 = 8
So 54576-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16S/c1-4-10(3)12-11-7-5-9(2)6-8-11/h5-8,10H,4H2,1-3H3
54576-40-8Relevant academic research and scientific papers
Reductive α-substitution of sulfoxides with grignard reagents promoted by a magnesium amide
Kobayashi, Kazuhiro,Yokota, Kouichi,Akamatsu, Hideki,Morikawa, Osamu,Konishi, Hisatoshi
, p. 441 - 443 (2007/10/03)
The reactions of sulfoxides bearing α-hydrogen(s) (RSOCHR1R2: R-alkyl or aryl; R1, R2 = H, alkyl, or aryl) with Grignard reagents (R3MgBr: R3 = Et, Ph, or vinyl) in the presence of the diisopropylaminomagnesium reagent, generated in situ by the treatment of diisopropylamine with the appropriate Grignard reagents in diethyl ether, have resulted in the formation of the corresponding sulfides (RSCR1R2R3) in moderate to good isolated yields.
Alkylation with Oxalic Esters. Scope and Mechanism.
Bergman, Jan,Norrby, Per-Ola,Sand, Peter
, p. 6113 - 6124 (2007/10/02)
Alkyl oxalates are well suited for use as standard synthetic reagents in N-, O-, or S-alkylations and often display an interesting regioselectivity.The mechanism seems to be a direct alkylation of the substrate anion.
