1191453-81-2 Usage
General Description
5-Chloro-1-Methyl-1H-pyrazol-3-aMine, also known as CM-pyrazole, is a chemical compound with the formula C4H6ClN3. It is a derivative of pyrazole and is commonly used as a building block in organic synthesis for the production of pharmaceuticals, agrochemicals, and other fine chemicals. The compound has been found to exhibit antimicrobial, antiviral, and anticancer activities, making it a valuable tool in drug discovery and development. Additionally, 5-Chloro-1-Methyl-1H-pyrazol-3-aMine has also been used in the synthesis of various heterocyclic compounds, making it an important intermediate in the chemical industry. Due to its versatile applications, this compound is widely utilized in research and development across various scientific disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 1191453-81-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,4,5 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1191453-81:
(9*1)+(8*1)+(7*9)+(6*1)+(5*4)+(4*5)+(3*3)+(2*8)+(1*1)=152
152 % 10 = 2
So 1191453-81-2 is a valid CAS Registry Number.
1191453-81-2Relevant articles and documents
SUBSTITUTED PYRIMIDINE COMPOUNDS, COMPOSITIONS AND MEDICINAL APPLICATIONS THEREOF
-
Paragraph 000153, (2015/03/13)
The present disclosure relates to pyrimidine compounds of formula (I), their stereoisomers, tautomers, pharmaceutically acceptable salts, polymorphs, solvates, and hydrates thereof. The present disclosure also relates to process of preparation of these pyrimidine compounds, and to pharmaceutical compositions containing them. The compounds of the present disclosure are useful in the treatment, prevention or suppression of diseases and disorders mediated by epidermal growth factor receptor (EGFR) family kinases.
8-substituted pyrazolopentathiepins and related compounds
-
, (2008/06/13)
Heteropentathiepins including pyrazolopentathiepins substituted in the 8-position; intermediate pyrazolo-1,2,3-thiadiazoles, pyrazolothiazathiolium chlorides, and 5-substituted aminopyrazoles; process for making the pentathiepins by reacting the corresponding 1,2,3-thiadiazoles with sulfur at elevated temperatures; process for making the thiazathiolium chlorides; and use of the pentathiepins as fungicides or as sulfur sensitizers in photographic emulsions.
