54675-18-2 Usage
Uses
Used in Pharmaceutical Industry:
4-Chloro-2-MethylaMino-benzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its role in creating compounds with therapeutic properties. Its potential as an anti-inflammatory and antineoplastic agent makes it valuable in developing new medications for treating inflammation and cancer.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Chloro-2-MethylaMino-benzoic acid serves as a crucial component in the production of pesticides and other agrochemicals, contributing to the development of effective solutions for crop protection and enhancement of agricultural yields.
Used in Dye and Pigment Production:
4-Chloro-2-MethylaMino-benzoic acid is utilized as a starting material in the manufacture of dyes and pigments, where its chemical properties allow for the creation of a wide range of colors and shades used in various industries, including textiles, plastics, and printing inks.
Used in Medicinal Chemistry Research:
As a compound with demonstrated potential in anti-inflammatory and antineoplastic activities, 4-Chloro-2-MethylaMino-benzoic acid is employed in research settings to explore its mechanisms of action and to develop new therapeutic agents for medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 54675-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54675-18:
(7*5)+(6*4)+(5*6)+(4*7)+(3*5)+(2*1)+(1*8)=142
142 % 10 = 2
So 54675-18-2 is a valid CAS Registry Number.
54675-18-2Relevant academic research and scientific papers
SELECTED BENZOFURAN DERIVATIVES
-
Page/Page column 19, (2008/06/13)
The invention relates to new benzofuran derivatives and their use as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical
COMPOSES SULFURES HETEROCYCLIQUES. XCVI. REACTION DE L'HYDRAZINE SUR LES DIHYDRO-1,2 BENZOTHIAZINE-3,1 THIONES-4
Legrand, Louis,Lozac'H, Noel
, p. 139 - 143 (2007/10/02)
1-Alkyl-1,2-dihydro-3,1-benzothiazine-4-thiones 1, when reacting with hydrazine, give with a good yield a 1-alkyl-3-amino-2,3-dihydro-1H-quinazoline-4-thione-2, often together with a derivative of 1,3,4-thiadiazole-3. With 1-aryl-1,2-dihydro-3,1-benzothiazine-4-thiones, the main product of the reaction with hydrazine appears to be a 1-aryl-4-hydrazono-1,4-dihydro-2H-3,1-benzothiazine 4, sometimes with some amount of 3.On the contrary, when reacting with hydrazine, 1-alkyl (or 1-aryl)-1,2-dihydro-3,1-benzothiazin-4-ones lead to a 2-alkylamino (or arylamino)-benzohydrazide 5. By thermolysis 4 isomerizes into 2 which is accompanied by derivatives (3 and 7) of 1,3,4-thiadiazole.The structures of compounds 2, 4 and 7 have been studied by NMR and UV spectrometry.