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76252-06-7

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  • Methanone,[3,4-dihydro-8-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]-1(2H)-quinolinyl]-3-pyridinyl-;76252-06-7

    Cas No: 76252-06-7

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  • Methanone,[3,4-dihydro-8-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]-1(2H)-quinolinyl]-3-pyridinyl-

    Cas No: 76252-06-7

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76252-06-7 Usage

Description

1,2,3,4-tetrahydro-8-[2-hydroxy-3-(isopropylamino)propoxy]-1-(3-pyridylcarbonyl)quinoline is a complex synthetic chemical compound that belongs to the quinoline family. It features a quinoline ring, a pyridylcarbonyl group, and an isopropylaminopropoxy side chain, which may contribute to its potential interactions with biological systems. Due to its structural similarity to other quinoline-based drugs with antimalarial and antiparasitic properties, this compound holds promise for pharmaceutical applications that require further research and testing to elucidate its specific pharmacological properties and potential medical uses.

Uses

Used in Pharmaceutical Industry:
1,2,3,4-tetrahydro-8-[2-hydroxy-3-(isopropylamino)propoxy]-1-(3-pyridylcarbonyl)quinoline is used as a potential pharmaceutical agent for its structural resemblance to quinoline-based drugs with established antimalarial and antiparasitic effects. The presence of hydroxy and isopropylamino groups suggests that it may engage in interactions with biological targets, which could be leveraged for therapeutic purposes.
Given the compound's potential for pharmaceutical applications, it may also be utilized in:
Antimalarial Applications:
As a derivative of quinoline, it could be developed into an antimalarial drug, targeting the Plasmodium parasites responsible for malaria.
Antiparasitic Applications:
Its structural features may allow it to combat various parasitic infections, similar to other quinoline-based antiparasitic drugs.
Drug Development Research:
For further exploration of its pharmacological properties, it may be used in research to identify specific mechanisms of action and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76252-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76252-06:
(7*7)+(6*6)+(5*2)+(4*5)+(3*2)+(2*0)+(1*6)=127
127 % 10 = 7
So 76252-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H27N3O3/c1-15(2)23-13-18(25)14-27-19-9-3-6-16-8-5-11-24(20(16)19)21(26)17-7-4-10-22-12-17/h3-4,6-7,9-10,12,15,18,23,25H,5,8,11,13-14H2,1-2H3

76252-06-7SDS

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 [8-[2-hydroxy-3-(propan-2-ylamino)propoxy]-3,4-dihydro-2H-quinolin-1-yl]-pyridin-3-ylmethanone

1.2 Other means of identification

Product number -
Other names Nicainoprolum

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:76252-06-7 SDS

76252-06-7Downstream Products

76252-06-7Relevant articles and documents

Boric acid catalyzed chemoselective reduction of quinolines

Adhikari, Priyanka,Bhattacharyya, Dipanjan,Das, Animesh,Konwar, Monuranjan,Nandi, Sekhar,Sarmah, Bikash Kumar

, p. 1214 - 1220 (2020/02/22)

Boric acid promoted transfer hydrogenation of substituted quinolines to synthetically versatile 1,2,3,4-tetrahydroquinolines (1,2,3,4-THQs) was described under mild reaction conditions using a Hantzsch ester as a mild organic hydrogen source. This methodology is practical and efficient, where isolated yields are excellent and reducible functional groups are well tolerated in the N-heteroarene moiety. The reaction parameters and tentative mechanistic pathways are demonstrated by various control experiments and NMR studies. The present work can also be scaled up to obtain gram quantities and the utility of the developed process is illustrated by the transformation of 1,2,3,4-THQs into a series of biologically important molecules including the antiarrhythmic drug nicainoprol.

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