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Ethanamine, 2-[(diphenylmethyl)thio]-N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27925-76-4

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27925-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27925-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,2 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27925-76:
(7*2)+(6*7)+(5*9)+(4*2)+(3*5)+(2*7)+(1*6)=144
144 % 10 = 4
So 27925-76-4 is a valid CAS Registry Number.

27925-76-4SDS

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-benzhydrylsulfanyl-N,N-dimethylethanamine

1.2 Other means of identification

Product number -
Other names (2-Benzhydrylmercapto-aethyl)-dimethyl-amin

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:27925-76-4 SDS

27925-76-4Relevant academic research and scientific papers

SARs at the monoamine transporters for a novel series of modafinil analogues

Cao, Jianjing,Prisinzano, Thomas E.,Okunola, Oluyomi M.,Kopajtic, Theresa,Shook, Matthew,Katz, Jonathan L.,Newman, Amy Hauck

, p. 48 - 52 (2011/04/22)

A series of modafinil (1) analogues were synthesized wherein (1) para-halo-substitutents were added to the aryl rings, (2) the sulfoxide function was removed, and (3) the primary amide group was replaced with secondary and tertiary amides and amines to investigate the effects of these chemical modifications on dopamine transporter, serotonin transporter, and norepinephrine transporter binding. In addition, the locomotor-stimulant effects in mice of (±)-modafinil (1), its R-and S-enantiomers, and its para-chloro sulfinylacetamide analogue (5c) were compared to those of cocaine.

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