1848-41-5 Usage
General Description
3-methoxy-1H-indazole, also known as 3-MeO-indazole, is a chemical compound with the molecular formula C9H8N2O. It belongs to the class of indazole compounds, which are organic heterocyclic molecules containing a five-membered ring with two nitrogen atoms. 3-methoxy-1H-indazole is a white to off-white crystalline powder with a molecular weight of 160.17 g/mol. It is commonly used in the field of organic chemistry as a precursor in the synthesis of various pharmaceuticals and other organic compounds. This chemical has also been studied for its potential as a psychedelic drug and has been the subject of research into its effects on the central nervous system. However, its precise pharmacological and toxicological properties have not been fully elucidated.
Check Digit Verification of cas no
The CAS Registry Mumber 1848-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1848-41:
(6*1)+(5*8)+(4*4)+(3*8)+(2*4)+(1*1)=95
95 % 10 = 5
So 1848-41-5 is a valid CAS Registry Number.
1848-41-5Relevant articles and documents
SELECTIVE INHIBITORS OF CLINICALLY IMPORTANT MUTANTS OF THE EGFR TYROSINE KINASE
-
, (2019/01/21)
The present invention provides compounds of Formula (I) or a subgeneric structure or species thereof, or a pharmaceutically acceptable salt, ester, solvate, and/or prodrug thereof, and methods and compositions for treating or ameliorating abnormal cell pr
Aromatic Diazonium Salts, X. - A One-Pot Procedure for the Jacobson Synthesis of Indazole
Ruechardt, Christoph,Hassmann, Volker
, p. 908 - 927 (2007/10/02)
Procedures are described for a one-pot synthesis of 1H-indazole and substituted indazoles 3 in good yield (Table 1) from o-toluidines 2, alkyl nitrite or nitrous oxides, potassium acetate, and acetic anhydride in benzene.The spectroscopic properties of substituted indazoles (Tables 2-4) are discussed. - 4-Phenylcinnoline (18) is prepared by the same procedure from o-(α-methylenebenzyl)aniline.
