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48133-71-7

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48133-71-7 Usage

General Description

2-[(2,6-DICHLOROBENZYL)THIO]ETHYLAMINE is a chemical compound with the molecular formula C10H14Cl2NS. It is an organic compound that contains a benzyl group, a thioether group, and an ethylamine group. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of the thioether group makes it useful in organic synthesis reactions, while the ethylamine group provides basic properties that make it suitable for use as a reagent in various chemical reactions. The 2,6-dichlorobenzyl group adds stability and contributes to the overall chemical properties and reactivity of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 48133-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,8,1,3 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 48133-71:
(7*4)+(6*8)+(5*1)+(4*3)+(3*3)+(2*7)+(1*1)=117
117 % 10 = 7
So 48133-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11Cl2NS/c10-8-2-1-3-9(11)7(8)6-13-5-4-12/h1-3H,4-6,12H2

48133-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2,6-dichlorophenyl)methylsulfanyl]ethanamine

1.2 Other means of identification

Product number -
Other names HMS550K01

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:48133-71-7 SDS

48133-71-7Downstream Products

48133-71-7Relevant articles and documents

A new strategy for the synthesis of β-benzylmercaptoethylamine derivatives

Ghosh, Subrata,Tochtrop, Gregory P.

supporting information; experimental part, p. 1723 - 1726 (2009/07/05)

Here, we describe a new experimental approach to the synthesis of the β-benzylmercaptoethylamine functionality, and illustrate its synthetic utility in multi-component reactions. Although prevalent in modern organic synthesis, no general methods have been described for this functionality. Using a carefully developed LiOH-water-ethanol reaction mixture, we were able to produce a diverse collection of β-benzylmercaptoethylamines containing a range of sensitive functional groups in excellent yields. To further illustrate their utility in molecular library synthesis, we also report the use of β-benzylmercaptoethylamines in five different multi-component reactions.

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