Welcome to LookChem.com Sign In|Join Free
  • or
4-METHYLQUINOLINE-2-CARBOXYLIC ACID is an organic compound with the molecular formula C10H9NO2. It is a derivative of quinoline-2-carboxylic acid, featuring a methyl group at the 4th position. 4-METHYLQUINOLINE-2-CARBOXYLIC ACID is known for its potential applications in various industries due to its unique chemical properties.

40609-76-5

Post Buying Request

40609-76-5 Suppliers

Recommended suppliers

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

40609-76-5 Usage

Uses

Used in Organic Synthesis:
4-METHYLQUINOLINE-2-CARBOXYLIC ACID is used as a building block for organic synthesis processes. Its unique structure allows it to be a valuable component in the creation of more complex organic molecules, which can be utilized in various applications such as pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 40609-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,0 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40609-76:
(7*4)+(6*0)+(5*6)+(4*0)+(3*9)+(2*7)+(1*6)=105
105 % 10 = 5
So 40609-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-7-6-10(11(13)14)12-9-5-3-2-4-8(7)9/h2-6H,1H3,(H,13,14)

40609-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methylquinoline-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-quinoline-2-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:40609-76-5 SDS

40609-76-5Downstream Products

40609-76-5Relevant academic research and scientific papers

Preparation of 4,7-diphenyl-1,10-phenanthroline-2,9-dicarboxylic acid catalyzed by iron(III)porphyrins with (diacetoxyiodo)benzene

Zhong, Qi-Di,Xue, Yun-Zhou,Yan, Hong,Song, Xiu-Qing,Zhong, Ru-Gang

body text, p. 5532 - 5535 (2010/12/20)

Using iron(III)porphyrins in combination with (diacetoxyiodo)benzene allows for the conversion of 2,9-bis(bromomethyl)-4,7-diphenyl-1,10-phenanthroline into 4,7-diphenyl-1,10-phenanthroline-2,9-dicarboxylic acid. This method provides a cost-effective and environmentally-friendly oxidation procedure using less toxic PhI(OAc)2 and biologically relevant iron(III)porphyrins. The catalytic activity of five kinds of iron-metallated functional porphyrins were investigated using different oxidants, including air, H2O 2, PhI(OAc)2, PhIO and NaClO. Our results showed that the use of T(p-NO2)PPFeCl with PhI(OAc)2 as the oxidant in the presence of water displays remarkable activity for the desired oxidation reaction. The generality of this method was examined by synthesizing the carboxylic acids of pyridines and quinolines.

STUDIES ON PYRIMIDINE DERIVATIVES. XXII. SITE-SELECTIVE OXIDATION OF DIMETHYLPYRIMIDINES WITH SELENIUM DIOXIDE TO PYRIMIDINE-MONOALDEHYDES

Sakamoto, Takao,Sakasai, Takeji,Yamanaka, Hiroshi

, p. 2485 - 2490 (2007/10/02)

The oxidation of 2,4-dimethylquinoline and its 1-oxide with an equimolecular amount of selenium dioxide in boiling dioxane afforded 4-methylquinoline-2-carbaldehyde and its 1-oxide, respectively.This oxidation was applicable to the selective preparation o

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 40609-76-5