Welcome to LookChem.com Sign In|Join Free
  • or
2-Methyl-6-quinolinecarboxylic acid is an organic compound with the molecular formula C11H9NO2. It is a derivative of quinoline carboxylic acids and possesses a methyl group at the 2nd position and a carboxylic acid group at the 6th position. 2-Methyl-6-quinolinecarboxylic acid is known for its potential applications in various fields, particularly as a precursor in the synthesis of biologically active molecules.

635-80-3

Post Buying Request

635-80-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

635-80-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Methyl-6-quinolinecarboxylic acid is used as a key intermediate in the synthesis of arylpyrazolopyridine derivatives, which are known as monoacylglycerol lipase modulators. These modulators have potential applications in the treatment of various diseases, including metabolic disorders and inflammatory conditions, by regulating the activity of monoacylglycerol lipase enzymes.

Check Digit Verification of cas no

The CAS Registry Mumber 635-80-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 635-80:
(5*6)+(4*3)+(3*5)+(2*8)+(1*0)=73
73 % 10 = 3
So 635-80-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-7-2-3-8-6-9(11(13)14)4-5-10(8)12-7/h2-6H,1H3,(H,13,14)

635-80-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H63790)  2-Methylquinoline-6-carboxylic acid, 97%   

  • 635-80-3

  • 1g

  • 210.0CNY

  • Detail
  • Alfa Aesar

  • (H63790)  2-Methylquinoline-6-carboxylic acid, 97%   

  • 635-80-3

  • 5g

  • 785.0CNY

  • Detail
  • Alfa Aesar

  • (H63790)  2-Methylquinoline-6-carboxylic acid, 97%   

  • 635-80-3

  • 25g

  • 3136.0CNY

  • Detail

635-80-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-6-Quinolinecarboxylic Acid

1.2 Other means of identification

Product number -
Other names 2-Methylquinoline-6-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:635-80-3 SDS

635-80-3Relevant academic research and scientific papers

Indenoquinaldine-Based Unsymmetrical Squaraine Dyes for Near-Infrared Absorption: Investigating the Steric and Electronic Effects in Dye-Sensitized Solar Cells

Bisht, Rajesh,Mele Kavungathodi, Munavvar Fairoos,Nithyanandhan, Jayaraj

, p. 16368 - 16378 (2018)

A series of near-infrared (NIR)-responsive unsymmetrical squaraine dyes (ISQ1–3) incorporating a fused indenoquinaldine-based donor have been designed and synthesized. C12 alkyl chains were incorporated at the sp3-hybridized carbon center of the indene unit of the indenoquinaldine in an out-of-plane orientation to control dye aggregation on the surface of titanium dioxide, and indole (ISQ1), benzo[e]indole (ISQ2), and quinoline (ISQ3) moieties were included as the donor component bearing the anchoring carboxy group to extend the absorption in the NIR region and to systematically study the effect of the electronic modification on the performance of dye-sensitized solar cells (DSSC). All the dyes exhibit intense absorption (?≥105 m?1 cm?1) in the NIR region, and the dye-adsorbed TiO2 films exhibit broad panchromatic absorption. The incident photon-to-current efficiency (IPCE) spectrum of the ISQ3-based DSSC device displays a panchromatic IPCE response up to 880 nm. Additionally, the ISQ3-sensitized device provides the best efficiency of 4.15 % with a short circuit current density (JSC) of 10.02 mA cm?2, open-circuit voltage (VOC) of 0.58 V, and fill factor (ff) of 72 % in the presence of 10 equivalents of 3α,7α-dihydroxy-5β-cholanic acid (CDCA). Electrochemical impedance spectroscopy analysis showed attenuated charge recombination in the ISQ3-sensitized DSSC, which contributes to its higher value of VOC compared with the other dyes.

Molecular structure, FT-IR, FT-Raman, NBO, HOMO and LUMO, MEP, NLO and molecular docking study of 2-[(E)-2-(2-bromophenyl)ethenyl]quinoline-6-carboxylic acid

Ulahannan, Rajeev T.,Panicker, C. Yohannan,Varghese, Hema Tresa,Musiol, Robert,Jampilek, Josef,Van Alsenoy, Christian,War, Javeed Ahmad,Srivastava

, p. 184 - 197 (2015)

The optimized molecular structure, vibrational frequencies, corresponding vibrational assignments of 2-[(E)-2-(2-bromophenyl)ethenyl]quinoline-6-carboxylic acid have been investigated experimentally and theoretically using Gaussian09 software package. Pot

NOVEL 3,5-DISUBSTITUTED-3H-IMIDAZO[4,5-B]PYRIDINE AND 3,5- DISUBSTITUTED -3H-[1,2,3]TRIAZOLO[4,5-B] PYRIDINE COMPOUNDS AS MODULATORS OF C-MET PROTEIN, ETC

-

Paragraph 0524, (2015/03/04)

The present invention provides compounds useful as c-Met protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of c-Met kinase mediated disease or disorders with them.

NOVEL 3,5-DISUBSTITUED-3H-IMIDAZO[4,5-B]PYRIDINE AND 3,5- DISUBSTITUED -3H-[1,2,3]TRIAZOLO[4,5-B] PYRIDINE COMPOUNDS AS MODULATORS OF C-MET PROTEIN KINASES

-

Paragraph 252, (2013/10/21)

The present invention provides compounds useful as C-met protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of C-met kinase mediated diseases or disorders with them.

Unsymmetrical squaraines incorporating quinoline for near infrared responsive dye-sensitized solar cells

Li, Jheng-Ying,Chen, Chia-Yuan,Ho, Wen-Chein,Chen, Szu-Han,Wu, Chun-Guey

, p. 5420 - 5423 (2013/01/15)

Two new unsymmetrical squaraines (WCH-SQ10 and WCH-SQ11), wherein the electron-rich 3,4-ethylenedioxy-thiophene conjugated fragment was linked unconventionally to the squaraine core and triphenyl amine donor, and carboxylic acid substituted quinoline was

Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines

Podeszwa,Niedbala,Polanski,Musiol,Tabak,Finster,Serafin,Milczarek,Wietrzyk,Boryczka,Mol,Jampilek,Dohnal,Kalinowski,Richardson

, p. 6138 - 6141 (2008/03/11)

The structure-activity relationships of new quinoline based compounds were investigated. Quinoline-5,8-dione and styrylquinoline scaffolds were used for the design of potentially active compounds. The novel analogues had comparable antiproliferative activ

BICYCLIC IMIDAZOL DERIVATIVES AGAINST FLAVIVIRIDAE

-

Page/Page column 97; 131, (2008/06/13)

Disclosed are compounds, compositions and methods for treatingFlaviviridae family virus infections.

Use of the Kohonen neural network for rapid screening of ex vivo anti-HIV activity of styrylquinolines

Polanski, Jaroslaw,Zouhiri, Fatima,Jeanson, Laurence,Desma?le, Didier,D'Angelo, Jean,Mouscadet, Jean-Fran?ois,Gieleciak, Rafal,Gasteiger, Johann,Le Bret, Marc

, p. 4647 - 4654 (2007/10/03)

Using the Kohonen neural network, the electrostatic potentials on the molecular surfaces of 14 styrylquinoline derivatives were drawn as comparative two-dimensional maps and compared with their known human immunodeficiency virus (HIV)-1 replication blocki

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 635-80-3