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N-[2-(4-nitrophenyl)ethyl]propan-1-amine is an organic compound with the molecular formula C11H16N2O2. It is a derivative of propan-1-amine, featuring a 4-nitrophenylethyl group attached to the nitrogen atom. N-[2-(4-nitrophenyl)ethyl]propan-1-amine is characterized by its amine functional group and a nitro group on the phenyl ring, which contributes to its chemical reactivity and properties. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and chemical intermediates. Due to its potential reactivity with other chemicals, it is important to handle N-[2-(4-nitrophenyl)ethyl]propan-1-amine with care, following appropriate safety protocols.

5339-13-9

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5339-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5339-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5339-13:
(6*5)+(5*3)+(4*3)+(3*9)+(2*1)+(1*3)=89
89 % 10 = 9
So 5339-13-9 is a valid CAS Registry Number.

5339-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-propyl-2-(4-nitrophenyl)-ethylamine

1.2 Other means of identification

Product number -
Other names dimethyl[2-(4-nitrophenyl)ethyl]propanedioate

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:5339-13-9 SDS

5339-13-9Relevant academic research and scientific papers

SIGMA-1 RECEPTOR LIGANDS AND METHODS OF USE

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Page/Page column 42-43, (2010/07/10)

The invention provides compounds of formula I and compositions thereof. The invention further provides methods of using the compounds and compositions. The compounds of the invention can provide high affinity binding to sigma-1 receptors in a mammal. The compounds can exhibit selectivity for the sigma-1 receptor over the sigma-2 receptor. The compounds and compositions of the invention can also be used to treat conditions that involve the sigma-1 receptor, such as addiction, cardiovascular conditions, and cancer, for example, cancer of the breast, lung, prostate, ovarian, colorectal, or the CNS.

Synthesis and characterization of N,N-dialkyl and N-alkyl-N-aralkyl fenpropimorph-derived compounds as high affinity ligands for sigma receptors

Hajipour, Abdol R.,Fontanilla, Dominique,Chu, Uyen B.,Arbabian, Marty,Ruoho, Arnold E.

experimental part, p. 4397 - 4404 (2010/09/12)

The sigma-1 receptor is a unique non-opioid, non-PCP binding site that has been implicated in many different pathophysiological conditions including psychosis, drug addiction, retinal degeneration and cancer. Based on the structure of fenpropimorph, a hig

PHENYLSULFONAMIDE-PHENYLETHYLAMINES USEFUL AS DOPAMINE RECEPTORS

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Page/Page column 6, (2008/06/13)

Compounds of Formula I and their pharmaceutically acceptable salts having selective dopamine D3 receptor activity suitable for treating central nervous system disorders. Formula I: R1 is independently H or a C1-C8 alkyl including isomeric forms thereof; R

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