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2-Chloroquinoline-6-carbonitrile, a member of the quinoline family, is a chemical compound with the molecular formula C10H5ClN2. It features a chlorine atom and a carbonitrile group, contributing to its versatility in organic synthesis. 2-CHLOROQUINOLINE-6-CARBONITRILE is known for its ability to undergo various chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.

78060-54-5

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78060-54-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloroquinoline-6-carbonitrile is used as an intermediate in the production of antimalarial drugs. Its unique structure allows for the development of new therapeutic agents that can combat malaria, a significant global health concern.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloroquinoline-6-carbonitrile serves as a key intermediate for the synthesis of insecticides. Its incorporation into these products helps in the development of effective crop protection solutions, ensuring agricultural productivity and food security.
Overall, 2-Chloroquinoline-6-carbonitrile's potential for the development of new therapeutic agents and crop protection products makes it a valuable compound in the fields of medicinal and agricultural chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 78060-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,6 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78060-54:
(7*7)+(6*8)+(5*0)+(4*6)+(3*0)+(2*5)+(1*4)=135
135 % 10 = 5
So 78060-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H5ClN2/c11-10-4-2-8-5-7(6-12)1-3-9(8)13-10/h1-5H

78060-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLOROQUINOLINE-6-CARBONITRILE

1.2 Other means of identification

Product number -
Other names 6-Quinolinecarbonitrile,2-chloro

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:78060-54-5 SDS

78060-54-5Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AND USES THEREOF

-

, (2021/07/31)

Provided herein are novel heterocyclic compounds, for example, compounds having Formula I, I-P, II, lI-P, or III. Also provided herein are pharmaceutical compositions comprising the compounds and methods of using the same, for example, in inhibiting aldehyde dehydrogenases and/or for treating various cancers, cancer metastasis, type 2 diabetes, pulmonary arterial hypertension (PAH) or neointimal hyperplasia (NIH).

UREA AND THIOUREA SUBSTITUTED BICYCLES DERIVATIVES AS PESTICIDES

-

Page/Page column 54, (2018/02/20)

The present invention relates to compounds of formula (I) a compound of formula (1') as defined herein, to processes for preparing them, to pesticidal, in particular insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising them and

INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

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Page/Page column 19, (2013/05/21)

The present invention provides compounds of Formula I I and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds act as diuretics and natriuretics and are valuable pharmaceutically active compounds for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension and conditions resulting from excessive salt and water retention.

2-(4-Alkylpiperazin-1-yl)quinolines as a new class of imidazole-free histamine H3 receptor antagonists

Zaragoza, Florencio,Stephensen, Henrik,Peschke, Bernd,Rimvall, Karin

, p. 306 - 311 (2007/10/03)

With the aim of identifying structurally novel, centrally acting histamine H3 antagonists, a series of 2-(4-alkylpiperazin-1-yl)quinolines was prepared. Systematic variation of the substituents led to highly potent histamine H3 antagonists with low polar surface area and appropriate log P for blood-brain barrier penetration.

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