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N2,N2-diMethylpyridine-2,6-diaMine, with the molecular formula C7H11N3, is a chemical compound that serves as a versatile building block in organic synthesis and pharmaceutical research. Characterized by its strong basic properties and the ability to form stable complexes with metal ions, N2,N2-diMethylpyridine-2,6-diaMine is also utilized as a ligand in coordination chemistry. Its applications extend to the production of pharmaceuticals and agrochemicals, making it an important intermediate in various chemical processes.

63763-86-0

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63763-86-0 Usage

Uses

Used in Organic Synthesis:
N2,N2-diMethylpyridine-2,6-diaMine is used as a building block for the synthesis of various organic compounds, contributing to the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In pharmaceutical research, N2,N2-diMethylpyridine-2,6-diaMine is employed as a key intermediate in the production of pharmaceuticals, aiding in the creation of novel drugs and therapeutic agents.
Used in Coordination Chemistry:
As a ligand in coordination chemistry, N2,N2-diMethylpyridine-2,6-diaMine is used to form stable complexes with metal ions, which can be applied in various chemical and catalytic processes.
Used in Agrochemical Production:
N2,N2-diMethylpyridine-2,6-diaMine is also utilized as an important intermediate in the production of agrochemicals, playing a role in the development of new pesticides and other agricultural products.

Check Digit Verification of cas no

The CAS Registry Mumber 63763-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63763-86:
(7*6)+(6*3)+(5*7)+(4*6)+(3*3)+(2*8)+(1*6)=150
150 % 10 = 0
So 63763-86-0 is a valid CAS Registry Number.

63763-86-0SDS

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 2-amino-6-N,N-dimethylamino pyridine

1.2 Other means of identification

Product number -
Other names 6-dimethylamino-2-amino pyridine

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:63763-86-0 SDS

63763-86-0Downstream Products

63763-86-0Relevant academic research and scientific papers

QUINAZOLINE DERIVATIVES

-

Page/Page column 132, (2008/06/13)

The invention concerns quinazoline derivatives of Formula (I) or a pharmaceutically-acceptable salt, solvate or pro-drug thereof, wherein each of X1, p, R1, q, R2, R3, R4, R5, Ring A, r and R6 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders or in the treatment of disease states associated with angiogenesis and/or vascular permeability.

EFFECT OF SUBSTITUENTS ON CHEMICAL SHIFT OF PROTONS OF THE AMINO GROUP IN PMR SPECTRA OF SUBSTITUTED AMINOPYRIDINES

Shkurko, O. P.,Mamaev, V. P.

, p. 47 - 52 (2007/10/02)

The effect of substituents on the chemical shift of the protons of the amino group in six series of m- and p-substituted 2-, 3- and 4-aminopyridines (in DMSO) was studied by correlation analysis using the inductive and resonance constants.The peculiarities of the pyridine ring in the transmission of the electronic effects of the substituents are discussed.

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