6245-57-4 Usage
Description
4-Methoxy-2-methylbenzoic acid is an organic compound with the chemical formula C8H8O3. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 106-110°C. 4-Methoxy-2-methylbenzoic acid is characterized by the presence of a methoxy group (-OCH3) at the 4-position and a methyl group (-CH3) at the 2-position on a benzene ring, with a carboxylic acid (-COOH) group attached to the benzene ring.
Uses
Used in Chemical Synthesis:
4-Methoxy-2-methylbenzoic acid is used as a key intermediate in the synthesis of various organic compounds, including 4-methoxy-2-methylbenzoates of Y(III) and lanthanides (III) (La to Lu, excluding Pm). These metal complexes have potential applications in various fields, such as catalysis, materials science, and as contrast agents in medical imaging.
Additionally, 4-Methoxy-2-methylbenzoic acid is used in the synthesis of 4-methoxy-2-methylbenzoic acid hydrazide and 5-bromo-4-methoxy-2-methylbenzoic acid. These derivatives can be further utilized in the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
4-Methoxy-2-methylbenzoic acid and its derivatives may have potential applications in the pharmaceutical industry as active pharmaceutical ingredients (APIs) or as intermediates in the synthesis of APIs. 4-Methoxy-2-methylbenzoic acid's unique structure and functional groups can be exploited to design and develop new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Methoxy-2-methylbenzoic acid and its derivatives can be used as active ingredients in the development of new pesticides, herbicides, or insecticides. 4-Methoxy-2-methylbenzoic acid's chemical properties can be tailored to target specific pests or weeds, providing effective and environmentally friendly solutions for agriculture.
Used in Materials Science:
4-Methoxy-2-methylbenzoic acid and its metal complexes can be employed in materials science for the development of new materials with unique properties. These materials can be used in various applications, such as sensors, catalysts, or advanced materials for energy storage and conversion.
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)
6245-57-4Relevant 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.
Site- and regio-selective incorporation of carbon dioxide into the C(sp2)Si bond of benzosilacyclobutenes
Ishida, Naoki,Okumura, Shintaro,Murakami, Masahiro
, p. 570 - 572 (2018/04/12)
A reaction of benzosilacyclobutenes with carbon dioxide is catalyzed by a nickel complex having an N-heterocyclic carbene ligand. Carbon dioxide inserts into the C(sp2)Si bond in a site- and regio-selective manner to form a carboncarbon bond, furnishing benzoic acid derivatives.
DMSO/I2 mediated C-C bond cleavage of α-ketoaldehydes followed by C-O bond formation: A metal-free approach for one-pot esterification
Venkateswarlu, Vunnam,Aravinda Kumar,Gupta, Sorav,Singh, Deepika,Vishwakarma, Ram A.,Sawant, Sanghapal D.
, p. 7973 - 7978 (2015/07/27)
A novel and efficient I2/DMSO mediated metal-free strategy is presented for the direct C-C bond cleavage of aryl-/heteroaryl- or aliphatic α-ketoaldehydes by C2-decarbonylation and C1-carbonyl oxidation to give the corresponding carboxylic acids followed by esterification in one pot, offering excellent yields in both the steps. Here, DMSO acts as the oxygen source/oxidant and this reaction works very well under both conventional heating and microwave irradiation. This is a very simple and convenient protocol.
