120422-90-4 Usage
Uses
Used in Pharmaceutical Industry:
4,6-dichloro-3-Methyl-1H-pyrazolo[4,3-c]pyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
4,6-dichloro-3-Methyl-1H-pyrazolo[4,3-c]pyridine is also used in the agrochemical industry for the development of new pesticides and herbicides. Its specific properties and reactivity make it a promising candidate for the creation of effective and targeted agrochemicals.
Used in Research and Development:
4,6-dichloro-3-Methyl-1H-pyrazolo[4,3-c]pyridine is utilized in research and development for the study of pyrazolopyridine chemistry and its potential applications in various industries. Its unique structure and properties make it an important compound for understanding the reactivity and behavior of pyrazolopyridine compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 120422-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 120422-90:
(8*1)+(7*2)+(6*0)+(5*4)+(4*2)+(3*2)+(2*9)+(1*0)=74
74 % 10 = 4
So 120422-90-4 is a valid CAS Registry Number.
120422-90-4Relevant articles and documents
PYRAZOLYL-SUBSTITUTED HETEROARYLS AND THEIR USE AS MEDICAMENTS
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, (2017/03/28)
The invention relates to new substituted heteroaryls of formula 1 or of formula 1' wherein A is either N or CH, wherein R2 is selected from the group consisting of -C1-3-alkyl, -C1-3-haloalkyl, F, Br, CI, wherein Y is selected from -O- or -CH2-, and wherein R3 is defined as in claim 1, and the pharmaceutically acceptable salts thereof, and the use of these aforementioned compounds for the treatment of diseases such as asthma, COPD, allergic rhinitis, allergic dermatitis, lupus erythematodes, lupus nephritis and rheumatoid arthritis.
PYRAZOLOPYRIDINES AS INHIBITORS OF THE KINASE LRRK2
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, (2011/12/02)
A compound of formula la or formula lb, or a pharmaceutically acceptable salt or ester thereof, wherein R1 is selected from: aryl; heteroaryl; -NHR3; fused aryl-C4-7-heterocycloalkyl; - CONR4R5; -NHCO
Photochemical rearrangements of 3-methyliscxazolopyridines
Donati, Donato,Fusi, Stefania,Ponticelli, Fabio,Tedeschi, Piero
, p. 1899 - 1905 (2007/10/02)
Irradiation in water-saturated ethyl ether of isoxazolopyridines 1a,e, beside the corresponding oxazolopyridines 2a,e, leads to N-methylcarboxamides 3a,e via 1-2 shift of the methyl group. The isoxazolopyridine 5, bearing a hydrazino group in 4-position, rearranges only to l-aminopyrazolopyridine 6.