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68621-16-9

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68621-16-9 Usage

Description

(3,4-Dichloro-benzyl)-ethyl-aMine, with the molecular formula C9H12Cl2N, is a chemical compound that is a derivative of benzylamine, featuring two chlorine atoms attached to the benzene ring. (3,4-Dichloro-benzyl)-ethyl-aMine is recognized for its role as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a building block in organic synthesis for creating a variety of chemical compounds. Its applications extend to research and development within the pharmaceutical and agricultural sectors, and it may also contribute to the production of dyes and pigments, highlighting its importance across multiple industries.

Uses

Used in Pharmaceutical Industry:
(3,4-Dichloro-benzyl)-ethyl-aMine is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, (3,4-Dichloro-benzyl)-ethyl-aMine serves as an intermediate, playing a crucial role in the creation of agrochemicals that can enhance crop protection and yield.
Used in Organic Synthesis:
(3,4-Dichloro-benzyl)-ethyl-aMine is utilized as a building block in organic synthesis, enabling the preparation of a diverse range of chemical compounds for various applications.
Used in Research and Development:
(3,4-Dichloro-benzyl)-ethyl-aMine is employed in research and development efforts within the pharmaceutical and agricultural industries to innovate and discover new product applications.
Used in Dyes and Pigments Production:
(3,4-Dichloro-benzyl)-ethyl-aMine may also be used in the production of dyes and pigments, indicating its potential for coloration applications in different industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 68621-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,2 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 68621-16:
(7*6)+(6*8)+(5*6)+(4*2)+(3*1)+(2*1)+(1*6)=139
139 % 10 = 9
So 68621-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H11Cl2N/c1-2-12-6-7-3-4-8(10)9(11)5-7/h3-5,12H,2,6H2,1H3

68621-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(3,4-dichlorophenyl)methyl]ethanamine

1.2 Other means of identification

Product number -
Other names ethyl-(3,4-dichloro-benzyl)-amine

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:68621-16-9 SDS

68621-16-9Downstream Products

68621-16-9Relevant articles and documents

COMPOSITION FOR DESTRUCTION OF MICROALGAE OR SPHAEROCARPUS

-

Paragraph 0132-0134, (2018/10/19)

The present disclosure relates to a composition for the destruction of microalgae or mosses. The composition for the destruction of microalgae or mosses may suppress the growth and proliferation of microalgae when treated in moss cultivation facilities, marine microalgae cultivation facilities, areas in which green or red tide is occurring, or areas in which green or red tide is expected to occur, thereby preventing damage caused by the green or red tide.

Benzylamines: Synthesis and evaluation of antimycobacterial properties

Meindl,Von Angerer,Schonenberger,Ruckdeschel

, p. 1111 - 1118 (2007/10/02)

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

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