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6245-57-4

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6245-57-4 Usage

Uses

4-Methoxy-2-methylbenzoic acid may be used in the synthesis of 4-methoxy-2-methylbenzoates of Y(III) and lanthanides (III) (La to Lu, excluding Pm). It may also be used to synthesize 4-methoxy-2-methylbenzoic acid hydrazide and 5-bromo-4-methoxy-2-methylbenzoic acid.

General Description

4-Methoxy-2-methylbenzoic acid (2-methylanisic acid) is a trisubstituted aromatic compound. It is a positional isomeric form of 2-methoxy-4-methylbenzoic acid. 4-Methoxy-2-methylbenzoic acid readily forms complexes with Mn(II), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II).

Check Digit Verification of cas no

The CAS Registry Mumber 6245-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6245-57:
(6*6)+(5*2)+(4*4)+(3*5)+(2*5)+(1*7)=94
94 % 10 = 4
So 6245-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c1-6-5-7(12-2)3-4-8(6)9(10)11/h3-5H,1-2H3,(H,10,11)

6245-57-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H27096)  4-Methoxy-2-methylbenzoic acid, 97%   

  • 6245-57-4

  • 1g

  • 420.0CNY

  • Detail
  • Alfa Aesar

  • (H27096)  4-Methoxy-2-methylbenzoic acid, 97%   

  • 6245-57-4

  • 5g

  • 1380.0CNY

  • Detail

6245-57-4SDS

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 4-METHOXY-2-METHYLBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Methyl-p-anisic 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:6245-57-4 SDS

6245-57-4Relevant articles and documents

Cyhalofop-containing pesticide composition and application thereof

-

, (2021/11/26)

The invention discloses a pesticide composition containing cyhalofop-butyl and application thereof, belongs to the technical field of pesticide preparation and comprises 10 - 20 parts of cyhalofop-butyl. Tetramethyl chloride 3-5 parts, synergistic microcapsule 8-13 parts, wetting agent 1.5 - 4.5 parts, dispersing agent 1-3 parts, defoaming agent 0.5 - 1.5 parts and water 40 - 50 parts. When the water in the soil is less, the weed is absorbed by the chitosan so as to accelerate the absorption of A the synergic microcapsule and the cyhalofop-butyl ester, so that the pesticide composition is greatly reduced per mu.

Chemical synthesis method of 6-bromo-5-hydroxyl iso-indolin-1-ketone

-

Paragraph 0007; 0023-0025; 0036-0038; 0049-0051, (2019/01/14)

The invention belongs to the field of chemical synthesis, and particularly relates to 6-bromo-5-hydroxyl iso-indolin-1-ketone as well as a chemical synthesis method thereof. A synthetic route of the method is as follows: (shown in the description). The ch

An outstanding catalyst for the oxygen-mediated oxidation of arylcarbinols, arylmethylene and arylacetylene compounds

Urgoitia,Sanmartin,Herrero,Domínguez

supporting information, p. 4799 - 4802 (2015/03/18)

A convenient and sustainable protocol for the aerobic oxidation of benzyl alcohols to carbonyl compounds, based on the use of 1,2,4-triazole-type ligands and nickel(ii) bromide, is described. This combination leads to the formation of an exceedingly active, enzyme-like system that allows for other oxidative processes, such as benzylic C-H oxidation and oxygen-mediated cleavage of C-C triple bond, a pioneering procedure for transformation of alkynes into carboxylic acids.

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