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52516-13-9

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52516-13-9 Usage

Description

1-(2,4-DICHLORO-PHENYL)-ETHYLAMINE, also known as 2,4-Dichlorophenethylamine, is an organic compound with the chemical formula C8H10Cl2N. It is a clear colorless to yellow liquid at room temperature and is commonly utilized as a synthetic intermediate in the pharmaceutical and chemical industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Synthesis:
1-(2,4-DICHLORO-PHENYL)-ETHYLAMINE is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its application in this industry is primarily due to its ability to react with other molecules to form new compounds with potential therapeutic properties.
1. Used in the Synthesis of cis-(L-Arginyl)amino-N-(2,4-dichlorophenylmethyl)-L-proline 2,4-dichlorophenethylamide:
In this application, 1-(2,4-DICHLORO-PHENYL)-ETHYLAMINE serves as a key component in the synthesis of a specific peptide derivative. 1-(2,4-DICHLORO-PHENYL)-ETHYLAMINE has potential applications in the treatment of various medical conditions, making the use of 2,4-Dichlorophenethylamine crucial in the development of new therapeutic agents.
2. Used in the Synthesis of Various N-alkylglycines:
1-(2,4-DICHLORO-PHENYL)-ETHYLAMINE is also employed in the synthesis of N-alkylglycines, a class of compounds with potential applications in the pharmaceutical industry. These compounds can be used as precursors for the development of new drugs or as active ingredients themselves, depending on their specific properties and potential therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 52516-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,1 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52516-13:
(7*5)+(6*2)+(5*5)+(4*1)+(3*6)+(2*1)+(1*3)=99
99 % 10 = 9
So 52516-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9Cl2N/c1-5(11)7-3-2-6(9)4-8(7)10/h2-5H,11H2,1H3

52516-13-9SDS

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 2,4-Dichlorophenethylamine

1.2 Other means of identification

Product number -
Other names 2-(2,4-Dichlorophenyl)ethylaMine

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:52516-13-9 SDS

52516-13-9Relevant articles and documents

Preparation method 5,7 - dichloro -1, 2, 3 and 4 - tetrahydroisoquinoline

-

Paragraph 0058-0062, (2021/08/25)

The invention provides a preparation method of 5, 7 - dichloro -1, 2, 3 and 4 - tetrahydroisoquinoline, which comprises the following steps: reducing 2, 4 - dichlorobenzene acetonitrile by first reducing agent to generate 2 and 4 - dichlorophenylethylamin

Synthesis and antioxidant characteristic of novel thiazolidinone derivatives

Amutha, Chinnadurai,Saravanan, Sivaperuman,Muthusubramanian, Shanmugam

, p. 377 - 383 (2014/05/06)

A series of novel thiazolidinone derivatives have been synthesized by solventless condensation of N-alkylamines with arylaldehydes at room temperature followed by a microwave assisted solventless addition of thioglycollic acid to the resultant imines. The synthesized compounds are characterized by 1H NMR, 13C NMR, MS and X-ray techniques and one of the synthesized thiazolidinones has been evaluated for its antioxidant property.

2-aminobenzoxazole derivatives and combinatorial libraries thereof

-

, (2008/06/13)

The present invention relates to novel 2-aminobenzoxazole derivative compounds of the following formula: wherein R1 to R4 and Z have the meanings provided herein. The invention further relates to combinatorial libraries containing two or more such compounds, as well as methods of preparing 2-aminobenzoxazole derivative compounds.

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