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2-(propylamino)isonicotinonitrile is a chemical compound with the molecular formula C10H13N3, derived from isonicotinic acid and featuring a propylamine group attached to the isonicotinonitrile structure. It is recognized for its versatile reactivity and potential as a building block in the synthesis of various biologically active molecules, making it a valuable asset in medicinal chemistry for the development of new drugs and chemical entities.

127680-76-6

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127680-76-6 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(propylamino)isonicotinonitrile is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the creation of biologically active molecules. Its chemical properties allow it to be a key component in the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 2-(propylamino)isonicotinonitrile serves as an intermediate, playing a crucial role in the synthesis of compounds that have applications in agriculture, such as pesticides and herbicides, due to its potential to form active ingredients with desired properties.
Used in Medicinal Chemistry Research:
2-(propylamino)isonicotinonitrile is utilized as a research tool in medicinal chemistry, where its reactivity and structural features are explored to understand and develop new chemical entities with therapeutic potential. Its role in this field is significant for advancing the discovery and design of novel pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 127680-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,8 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127680-76:
(8*1)+(7*2)+(6*7)+(5*6)+(4*8)+(3*0)+(2*7)+(1*6)=146
146 % 10 = 6
So 127680-76-6 is a valid CAS Registry Number.

127680-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(propylamino)pyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-(propylamino)isonicotinonitrile

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:127680-76-6 SDS

127680-76-6Downstream Products

127680-76-6Relevant academic research and scientific papers

Discovery of an N-(2-aminopyridin-4-ylmethyl)nicotinamide derivative: A potent and orally bioavailable NCX inhibitor

Kuramochi, Takahiro,Kakefuda, Akio,Yamada, Hiroyoshi,Tsukamoto, Issei,Taguchi, Taku,Sakamoto, Shuichi

, p. 4022 - 4036 (2007/10/03)

Ca2+ overload in myocardial cells is responsible for arrhythmia. Sodium-calcium exchanger (NCX) inhibitors are more effective than sodium-hydrogen exchanger (NHE) inhibitors with regard to modulation of Ca 2+ overload, because NCX inhibitors can directly inhibit the influx of Ca2+ into cells. NCX is an attractive target for the treatment of heart failure and ischemia-reperfusion. We have designed and synthesized a series of N-(2-aminopyridin-4-ylmethyl)nicotinamide derivatives, based on compound 5. We have discovered a novel NCX inhibitor (23h) with an IC 50 value of 0.12 μM against reverse NCX. The inhibitory activities of our NCX inhibitors against cytochrome P450 were also evaluated. The effects on heart failure and the pharmacokinetic profile of compound 23h are discussed.

A Study of the Photochemically Induced Reaction of Pyridine-2,4-dicarbonitrile with Primary and Secondary Amines. A Direct Synthesis of Aminocyanopyridines

Bernardi, Rosanna,Caronna, Tullio,Morrocchi, Sergio,Ursini, Maurizio,Vittimberga, Bruno M.

, p. 97 - 100 (2007/10/02)

A novel synthesis of alkylaminopyridinecarbonitriles by a photoinitiated substitution reaction between pyridine-2,4-dicarbonitrile and certain amines is described.The mechanism is discussed.

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