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n-(2,5-dichlorobenzyl)-n-methylamine, with the molecular formula C9H10Cl2N, is an organic compound derived from benzylamine and methylamine, featuring two chlorine atoms on the benzene ring. n-(2,5-dichlorobenzyl)-n-methylamine is recognized for its structural features and biological activity, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.

90390-16-2

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90390-16-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
n-(2,5-dichlorobenzyl)-n-methylamine is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its unique structure and reactivity facilitate the creation of diverse chemical entities with potential therapeutic and pesticidal properties.
Used in Disinfectant Products:
As an active ingredient in some disinfectant products, n-(2,5-dichlorobenzyl)-n-methylamine is utilized for its antimicrobial properties. It helps to eliminate harmful microorganisms, ensuring cleanliness and reducing the risk of infections in various settings.
Used in Medicinal Chemistry and Drug Development:
Due to its structural features and biological activity, n-(2,5-dichlorobenzyl)-n-methylamine has potential applications in the field of medicinal chemistry and drug development. Researchers can leverage its properties to design and synthesize novel compounds with improved pharmacological profiles, targeting a wide range of diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 90390-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,9 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90390-16:
(7*9)+(6*0)+(5*3)+(4*9)+(3*0)+(2*1)+(1*6)=122
122 % 10 = 2
So 90390-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9Cl2N/c1-11-5-6-4-7(9)2-3-8(6)10/h2-4,11H,5H2,1H3

90390-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name n-(2,5-dichlorobenzyl)-n-methylamine

1.2 Other means of identification

Product number -
Other names 2,5-Dichloro-N-methylbenzenemethanamine

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:90390-16-2 SDS

90390-16-2Upstream product

90390-16-2Downstream Products

90390-16-2Relevant academic research and scientific papers

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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