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1,4-DIMETHOXY-2-ETHYLTHIOBENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24920-39-6

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24920-39-6 Usage

Physical state

Colorless liquid

Odor

Faint

Primary uses

a. Production of fragrances and flavors
b. Intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds

Chemical classification

Thioether

Thioether definition

Contains a sulfur atom bonded to two organic groups

Safety precautions

a. Harmful if inhaled, swallowed, or absorbed through the skin
b. Can cause irritation to the eyes and skin

Handling

Handle with care to avoid exposure and potential health risks

Check Digit Verification of cas no

The CAS Registry Mumber 24920-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24920-39:
(7*2)+(6*4)+(5*9)+(4*2)+(3*0)+(2*3)+(1*9)=106
106 % 10 = 6
So 24920-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2S/c1-4-13-10-7-8(11-2)5-6-9(10)12-3/h5-7H,4H2,1-3H3

24920-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfanyl-1,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 2,5-dimethoxyphenyl ethyl sulfide

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:24920-39-6 SDS

24920-39-6Relevant academic research and scientific papers

Synthesis of deuterium labeled phenethylamine derivatives

Xu, Ya-Zhu,Chen, Chinpiao

, p. 1187 - 1200 (2008/04/18)

The synthesis of a series of five deuterium labeled phenethylamine derivatives, 4-bromo-2,5-[2H6]-dimethoxyphenethylamine (2C-B), 4-chloro-2,5-[2H6]-dimethoxyphenethylamine (2C-C), 2,5-[2H6]-dimethoxy-4-iodophenethylamine (2C-I), 2,5-[2H6]-dimethoxy-4-ethylthiophenethylamine (2C-T-2) and 2,5-[2H6]-dimethoxy-4-n-propylthiophenethylamine (2C-T-7) from 1,4-[2H6]-dimethoxybenzene is described. The isotopically labeled compounds are used as internal standards in gas chromatography-mass spectrometry (GC-MS) assays. Copyright

S-oxidation products of alkylthioamphetamines

Rezende, Marcos Caroli,Nunez, Christian,Sepulveda-Boza, Silvia,Cassels, Bruce K.,Hurtado-Guzman, Claudio

, p. 2741 - 2750 (2007/10/03)

The preparation of the sulfoxides and the sulfones of two centrally active alkylthioamphetamine salts, (±)-1-(4-methylthiophenyl)-2-aminopropane hydrochloride (2) (MTA · HCl) and (±)-1-(2,5-dimethoxy-4-ethylthiophenyl)-2-aminopropane hydrochloride (7) (AL

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