14290-92-7 Usage
Uses
Used in Flavoring Industry:
TERT-BUTYL ETHYL SULFIDE is used as a flavoring agent for its ability to impart specific aromas and tastes to food products. It is commonly found in items such as cheese, beer, and coffee, enhancing their flavor profiles and consumer appeal.
Used in Chemical Industry:
TERT-BUTYL ETHYL SULFIDE is used as a solvent for its capacity to dissolve various substances, facilitating chemical reactions and processes in the industry.
Used as a Chemical Intermediate:
In the production of other organic compounds, TERT-BUTYL ETHYL SULFIDE is utilized as a chemical intermediate, playing a crucial role in the synthesis of a range of chemical products.
Safety Considerations:
Due to its flammable nature and potential to cause respiratory and skin irritation upon prolonged exposure, TERT-BUTYL ETHYL SULFIDE should be handled with care. It is essential to store it in a cool, well-ventilated area to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 14290-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,9 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14290-92:
(7*1)+(6*4)+(5*2)+(4*9)+(3*0)+(2*9)+(1*2)=97
97 % 10 = 7
So 14290-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H14S/c1-5-7-6(2,3)4/h5H2,1-4H3
14290-92-7Relevant articles and documents
Indium-catalyzed reductive three-component coupling reaction of aliphatic/aromatic carboxylic acids with t-butyl mercaptan leading to unsymmetrical dialkyl sulfides
Sakai, Norio,Yoshimoto, Shunsuke,Miyazaki, Takahiro,Ogiwara, Yohei
supporting information, p. 3117 - 3120 (2016/07/06)
An InI3–TMDS (1,1,3,3-tetramethyldisiloxane) reducing system efficiently catalyzed a sequential three-component coupling of aliphatic carboxylic acids, aromatic carboxylic acids, and t-butyl mercaptan (t-butylthiol), to produce unsymmetrical dialkyl sulfides. With this reducing system, t-butyl mercaptan became a new source of sulfidation via an alkyl t-butyl sulfide that functioned as the reaction intermediate.
Preparation of Alkanesulfenamides by Selective Elimination of t-Butyl Group in S-Alkyl-S-t-butylsulfilimines
Yamamoto, Tamotsu,Kakimoto, Masa-aki,Maejima, Takeshi,Okawara, Makoto
, p. 1249 - 1250 (2007/10/02)
N-Tosylalkanesulfenamides have been prepared via the reaction of alkyl halides with 2-methyl-2-propanethiolate followed by S-imination with chloramine T and the thermolysis.This method comprises the use of selective elimination of t-butyl group in S-alkyl
