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14290-92-7

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14290-92-7 Usage

General Description

Tert-butyl ethyl sulfide is a chemical compound with the formula (C4H9)2S. It is a clear, colorless to pale yellow liquid with a characteristic odor. Tert-butyl ethyl sulfide is commonly used as a flavoring agent and is often found in food products such as cheese, beer, and coffee. It is also used as a solvent and as a chemical intermediate in the production of other organic compounds. Tert-butyl ethyl sulfide is flammable and can cause irritation to the respiratory system and skin upon prolonged exposure. It should be handled with care and stored in a cool, well-ventilated area.

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

14290-92-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfanyl-2-methylpropane

1.2 Other means of identification

Product number -
Other names Propane, 2-(ethylthio)-2-methyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14290-92-7 SDS

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.

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