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74209-44-2

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74209-44-2 Usage

Description

2,2-Diethoxy-2-(4-pyridyl)ethylamine is a chemical compound with the molecular formula C12H19NO2. It is a derivative of pyridine and is known for its ability to form stable complexes with various metal ions, making it useful in coordination chemistry and metal ion extraction processes. This versatile chemical is commonly used in organic synthesis and pharmaceutical research, as well as in the production of various pharmaceuticals and agrochemicals.

Uses

Used in Chemical Industry:
2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as a reagent in organic synthesis for its ability to form stable complexes with metal ions, which aids in various chemical reactions and processes.
Used in Pharmaceutical Research:
In pharmaceutical research, 2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as a building block for the development of new pharmaceuticals, leveraging its complex-forming properties to enhance drug design and effectiveness.
Used in Coordination Chemistry:
2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as a ligand in coordination chemistry to create stable metal complexes, which have potential applications in various fields such as catalysis, materials science, and medicinal chemistry.
Used in Metal Ion Extraction Processes:
In metal ion extraction processes, 2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as an extracting agent to selectively bind and separate metal ions from solutions, which is crucial in environmental remediation and industrial applications.
Used in Production of Pharmaceuticals:
2,2-Diethoxy-2-(4-pyridyl)ethylamine is used as an intermediate in the production of various pharmaceuticals, contributing to the synthesis of active ingredients and improving drug efficacy.
Used in Agrochemicals:
In the agrochemical industry, 2,2-Diethoxy-2-(4-pyridyl)ethylamine is used in the development of new agrochemicals, such as pesticides and herbicides, where its complex-forming ability can enhance the performance and selectivity of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 74209-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74209-44:
(7*7)+(6*4)+(5*2)+(4*0)+(3*9)+(2*4)+(1*4)=122
122 % 10 = 2
So 74209-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2O2/c1-3-14-11(9-12,15-4-2)10-5-7-13-8-6-10/h5-8H,3-4,9,12H2,1-2H3

74209-44-2SDS

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 2,2-diethoxy-2-pyridin-4-ylethanamine

1.2 Other means of identification

Product number -
Other names 2,2-diethoxy-2-pyridin-4-ylethylamine

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:74209-44-2 SDS

74209-44-2Relevant articles and documents

Efficient synthesis of 2-imidazol-2-ylacetates

Ha, Jae Du,Lee, Su Jung,Nam, So Yeun,Kang, Seung Kyu,Cho, Seung Yoon,Ahn, Jin Hee,Choi, Joong-Kwon

, p. 6201 - 6204 (2007/10/03)

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.

α-amino acetals: 2,2-Diethoxy-2-(4-pyridyl) ethylamine

LaMattina, John L.,Suleske

, p. 19 - 19 (2017/06/02)

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