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Ethanamine, N,N-diethyl-2-[(phenylmethyl)thio]-, also known as N,N-diethyl-2-(benzylthio)ethanamine, is an organic compound with the chemical formula C13H21NS. It is a colorless liquid with a molecular weight of 221.38 g/mol. Ethanamine, N,N-diethyl-2-[(phenylmethyl)thio]- is characterized by the presence of an ethanamine backbone, featuring two diethylamine groups attached to the nitrogen atom and a benzylthio group connected to the carbon atom at the second position. It is used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of pesticides and other specialty chemicals. Due to its reactivity and potential applications, it is essential to handle Ethanamine, N,N-diethyl-2-[(phenylmethyl)thio]- with care, adhering to proper safety protocols.

7708-55-6

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7708-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7708-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7708-55:
(6*7)+(5*7)+(4*0)+(3*8)+(2*5)+(1*5)=116
116 % 10 = 6
So 7708-55-6 is a valid CAS Registry Number.

7708-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzylsulfanyl-N,N-diethylethanamine

1.2 Other means of identification

Product number -
Other names Benzyldiethylaminoethylsulfid

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:7708-55-6 SDS

7708-55-6Relevant academic research and scientific papers

Synthesis of benzyl sulfidesviasubstitution reaction at the sulfur of phosphinic acid thioesters

Nishiyama, Yoshitake,Hosoya, Takamitsu,Yoshida, Suguru

supporting information, p. 5771 - 5774 (2020/06/03)

An ambident electrophilicity of phosphinic acid thioesters is disclosed. Unexpected carbon-sulfur bond formation took place in the reaction between phosphinic acid thioesters and benzyl Grignard reagents. The developed method for benzyl sulfides has a wide substrate scope and was applicable for the synthesis of a drug analog.

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