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2-CHLORO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBONITRILE is a quinoline derivative that features a carbonitrile group and a chlorine atom attached to a tetrahydroquinoline ring structure. This chemical compound is recognized for its unique reactivity and structural properties, which make it a significant intermediate in the synthesis of biologically active compounds and potential drugs.

65242-27-5

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65242-27-5 Usage

Uses

Used in Pharmaceutical Industry:
2-CHLORO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBONITRILE is used as a building block for the synthesis of various biologically active compounds due to its unique chemical structure and reactivity. It plays a crucial role in the development of complex pharmaceutical compounds, contributing to the advancement of new drug therapies.
Used in Research and Development:
In the field of organic synthesis and medicinal chemistry, 2-CHLORO-5,6,7,8-TETRAHYDROQUINOLINE-3-CARBONITRILE is utilized as a research chemical. Its properties are studied to understand its potential applications and to develop new methods for synthesizing related compounds, thereby expanding the scope of chemical research and innovation in medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 65242-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,4 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65242-27:
(7*6)+(6*5)+(5*2)+(4*4)+(3*2)+(2*2)+(1*7)=115
115 % 10 = 5
So 65242-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClN2/c11-10-8(6-12)5-7-3-1-2-4-9(7)13-10/h5H,1-4H2

65242-27-5SDS

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 2-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile

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:65242-27-5 SDS

65242-27-5Relevant academic research and scientific papers

Synthesis and Neurotropic Activity of New Pyrimido[4′,5′:4,5]Thieno[2,3-b]Quinoline Derivatives

Dabaeva,Bagdasaryan,Noravyan,Dzhagatspanyan,Nazaryan,Akopyan

, p. 587 - 591 (2015)

New methods for preparing pyrimido[4′,5′:4,5]thieno[2,3-b]quinoline derivatives based on 3-cyanohexahydro-2-quinoline were developed. The neurotropic activity of these compounds was studied.

Synthesis of 3-Amino-2-carboxamide Tetrahydropyrrolo[2,3- b ]quinolines

Pilkington, Lisa I.,Haverkate, Natalie A.,Van Rensburg, Michelle,Reynisson, Johannes,Leung, Euphemia,Barker, David

supporting information, p. 2811 - 2814 (2016/12/16)

This article communicates the first synthesis of 3-amino-2-carboxamide pyrrolo[2,3-b]quinolines and fused-ring pyrrolopyridines in an efficient synthesis via a Thorpe-Ziegler transformation. The reported synthetic route allows for a wide range of nitrogen analogues of thienopyridines - compounds which have potent bioactivities but poor aqueous solubility.

NOVEL BENZYLAMINE DERIVATIVES AS CETP INHIBITORS

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Page/Page column 244-245, (2008/06/13)

The present invention provides, among other things, new benzylamine compounds, compositions comprising benzylamine compounds, methods of making benzylamine compounds, and methods of using benzylamine compounds for treating or preventing a variety of conditions or diseases associated with lipoprotein metabolism.

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