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N-(3,5-dichlorobenzyl)pentan-1-amine is a chemical compound with the molecular formula C13H19Cl2N. It is a derivative of amine and contains a pentane backbone with a 3,5-dichlorobenzyl group attached. N-(3,5-dichlorobenzyl)pentan-1-amine is known for its potential applications in pharmaceutical and medical research, as well as in the field of organic chemistry.

90390-25-3

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90390-25-3 Usage

Uses

Used in Pharmaceutical and Medical Research:
N-(3,5-dichlorobenzyl)pentan-1-amine is used as an intermediate in the synthesis of various drugs and pharmaceuticals. Its unique structure allows it to be a valuable building block for the development of new molecules with therapeutic properties.
Used in Organic Chemistry:
In the field of organic chemistry, N-(3,5-dichlorobenzyl)pentan-1-amine may be utilized as a component in the creation of complex organic molecules, contributing to advancements in chemical research and development.
Used in Antimicrobial, Antifungal, and Antiviral Applications:
Due to its structural properties, N-(3,5-dichlorobenzyl)pentan-1-amine may exhibit antimicrobial, antifungal, and antiviral activities. This makes it a promising compound for scientific and medical studies aimed at developing new treatments and preventive measures against infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 90390-25-3 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, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90390-25:
(7*9)+(6*0)+(5*3)+(4*9)+(3*0)+(2*2)+(1*5)=123
123 % 10 = 3
So 90390-25-3 is a valid CAS Registry Number.

90390-25-3SDS

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 (3,5-Dichloro-benzyl)-pentyl-amine

1.2 Other means of identification

Product number -
Other names -

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:90390-25-3 SDS

90390-25-3Downstream Products

90390-25-3Relevant 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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