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3-Quinolinecarboxylic acid, 2-methyl-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10265-84-6

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10265-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10265-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10265-84:
(7*1)+(6*0)+(5*2)+(4*6)+(3*5)+(2*8)+(1*4)=76
76 % 10 = 6
So 10265-84-6 is a valid CAS Registry Number.

10265-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-4-phenyl-3-quinolinecarboxylic acid

1.2 Other means of identification

Product number -
Other names 2-methyl-4-phenylquinoline-3-carboxylic acid

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:10265-84-6 SDS

10265-84-6Relevant academic research and scientific papers

Synthesis and evaluation of novel triazolyl quinoline derivatives as potential antileishmanial agents

Upadhyay, Akanksha,Kushwaha, Pragati,Gupta, Sampa,Dodda, Ranga Prasad,Ramalingam, Karthik,Kant, Ruchir,Goyal, Neena,Sashidhara, Koneni V.

, p. 172 - 181 (2018)

The high potential of quinoline containing natural products and their derivatives in medicinal chemistry led us to discover novel series of 25 compounds for the development of new antileishmanial agents. A series of triazolyl 2-methyl-4-phenylquinoline-3-carboxylate derivatives has been synthesized via click chemistry inspired molecular hybridization approach and evaluated against Leishmania donovani. Most of the screened derivatives exhibited significant in vitro anti-leishmanial activity against promastigote (IC50 ranging from 2.43 to 45.75 μM) and intracellular amastigotes (IC50 ranging from 7.06 to 34.9 μM) than the control, miltefosine (IC50 = 8.4 μM), with less cytotoxicity in comparison to the standard drugs. Overall results revealed that prototype signify a new structural lead for antileishmanial chemotherapy.

Friedl?nder annulation: Scope and limitations of metal salt Lewis acid catalysts in selectivity control for the synthesis of functionalised quinolines

Tanwar, Babita,Kumar, Dinesh,Kumar, Asim,Ansari, Md. Imam,Qadri, Mohammad Mohsin,Vaja, Maulikkumar D.,Singh, Madhulika,Chakraborti, Asit K.

supporting information, p. 9824 - 9833 (2015/12/01)

The scope and limitations of metal salt Lewis acid catalysts were examined for the selectivity control for the formation of Friedl?nder and non-Friedl?nder products during the reaction involving 2-aminobenzophenone and ethyl acetoacetate. Among a pool of

Poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) and N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide as efficient reagents for synthesis of quinolines

Ghorbani-Vaghei, Ramin,Akbari-Dadamahaleh, Somayeh

scheme or table, p. 1055 - 1058 (2009/05/11)

Poly(N-bromo-N-ethylbenzene-1,3-disulfonamide) [PBBS] and N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide [TBBDA] were used as efficient reagents for the synthesis of quinolines in excellent yields from 2-aminoaryl ketones and carbonyl compounds under aqueo

Synthesis of 2-hydroxy-1,2,3,4-tetrahydroquinoline derivatives by a cyclocondensation reaction

Cremonesi, Giuseppe,Croce, Piero Dalla,Fontana, Francesco,La Rosa, Concetta

, p. 475 - 480 (2008/02/03)

The reaction of enolates (2) of 1,3-dicarbonyl compounds with N-(2-bromomethylphenyl)benzenesulfonamides (1) gives N-phenylsulfonyl-2-hydroxy-1,2,3,4-tetrahydroquinoline derivatives (3) whose structure and stereochemistry were assigned on the basis of ana

Mapping and fitting the peripheral benzodiazepine receptor binding site by carboxamide derivatives. Comparison of different approaches to quantitative ligand-receptor interaction modeling

Anzini,Cappelli,Vomero,Seeber,Menziani,Langer,Hagen,Manzoni,Bourguignon

, p. 1134 - 1150 (2007/10/03)

The synthetic-computational approach to the study of the binding site of peripheral benzodiazepine receptor (PBR) ligands related to 1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinolinecarboxamide (PK11195, 1) within their receptor (Cappelli et a

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