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69008-70-4

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69008-70-4 Usage

General Description

N,N-Dipropylpyridin-4-amine is a chemical compound with the molecular formula C12H19N. It is a derivative of pyridine with two propyl groups attached to the nitrogen atom at the 4-position. N,N-Dipropylpyridin-4-AMine is commonly used as a reactant in organic synthesis, often serving as a building block for various pharmaceutical drugs and agrochemicals. It has been found to exhibit anti-inflammatory and anti-thrombotic properties, making it potentially useful in the development of new medications for treating cardiovascular and inflammatory diseases. Additionally, it has been investigated for its potential to act as a corrosion inhibitor in industrial applications. Overall, N,N-Dipropylpyridin-4-amine is a versatile and interesting chemical with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 69008-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,0 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69008-70:
(7*6)+(6*9)+(5*0)+(4*0)+(3*8)+(2*7)+(1*0)=134
134 % 10 = 4
So 69008-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2/c1-3-9-13(10-4-2)11-5-7-12-8-6-11/h5-8H,3-4,9-10H2,1-2H3

69008-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dipropylpyridin-4-amine

1.2 Other means of identification

Product number -
Other names N,N-dipropylpyridin-4-amine

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:69008-70-4 SDS

69008-70-4Downstream Products

69008-70-4Relevant articles and documents

Method of synthesizing 4-alkylamino pyridine in mild condition

-

Paragraph 0020, (2018/01/17)

The invention discloses a method of synthesizing 4-alkylamino pyridine in a mild condition, and belongs to the technical field of organic synthesis. The method comprises performing a nucleophilic substitution reaction on 4-chloropyridine hydrochloride with alkyl amine in the presence of an inhibitor to prepare the 4-alkylamino pyridine, wherein the reaction temperature is in a range of 30-150 DEG C, the reaction time is in a range of 1-10 hours, the inhibitor is a fluoride salt, and the mass ratio of the inhibitor to the 4-chloropyridine hydrochloride is (0.1-1):1. In order to solve the problem of production safety hidden danger caused by a sharp rise of temperature in such kind of nucleophilic substitution reactions, the method provided by the invention introduces the inhibitor to control the reaction speed. With the addition of the inhibitor, the rise of the reaction temperature is effectively controlled, the reaction temperature and reaction speed are reduced to a controllable range, and thus the method provides possibility for safe production and is suitable for large-scale production. In addition, the synthetic reaction has only one step, the yield can reach 80%, and compared with the products of nucleophilic substitution reactions with no inhibitors, the product purity is increased and can reach 99% or more.

Preparation of the isomeric azaindoline family by intramolecular carbolithiation

Bailey, William F.,Salgaonkar, Paresh D.,Brubaker, Jason D.,Sharma, Vijayata

supporting information; body text, p. 1071 - 1074 (2009/04/06)

An operationally convenient, one-pot, three-step sequence has been developed that provides access to 3-substituted 4-, 5-, 6-, and 7-azaindolines (2,3-dihydro-1H-pyrollopyridines) via intramolecular carbolithiation of the aryllithium derived from an appro

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