1075-68-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Pyridazinamine, 3,6-dimethoxyis utilized as a key intermediate in the synthesis of various pharmaceuticals. Its role is pivotal for the development of new drugs, given its ability to participate in a range of chemical reactions that can lead to the creation of medicinally relevant compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Pyridazinamine, 3,6-dimethoxyis employed in the production of agrochemicals. Its reactivity and properties make it suitable for the synthesis of compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals to enhance crop protection and yield.
Used in Chemical Research and Development:
4-Pyridazinamine, 3,6-dimethoxyis also used as a building block in the research and development of new chemical compounds. Its potential biological activity and versatility in chemical reactions make it an attractive candidate for exploring novel applications and advancing the frontiers of chemical science.
Used in the Synthesis of Other Compounds:
4-Pyridazinamine, 3,6-dimethoxyis further utilized in the synthesis of other complex organic compounds, where its unique structure and reactivity contribute to the formation of new molecules with potential applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1075-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1075-68:
(6*1)+(5*0)+(4*7)+(3*5)+(2*6)+(1*8)=69
69 % 10 = 9
So 1075-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3O2/c1-10-5-3-4(7)6(11-2)9-8-5/h3H,1-2H3,(H2,7,8)
1075-68-9Relevant academic research and scientific papers
A new route to aminodiazines via metalation reaction. Synthesis of an aza analogue of Nevirapine: Diazines XV
Plé, Nelly,Turck, Alain,Couture, Karine,Quéguiner, Guy
, p. 838 - 842 (2007/10/03)
A new route to aminodiazines is reported, the ortho-directed lithiation of diazines is used, followed by reaction with tosyl azide as an electrophile. The reduction of the azido or tetrazolo compounds obtained was achieved and led to the expected amines. This methodology has allowed the synthesis of new aminodiazines and an improvement in the yield of various aminodiazines previously described. This reaction was used for the preparation of an aza analogue of Nevirapine.
Amination of 4-Nitropyridazine 1-Oxides by Liquid Ammonia/Potassium Permanganate
Tondys, Hanna,Plas, Henk C. van der
, p. 621 - 623 (2007/10/02)
Treatment of 4-nitropyridazine 1-oxide (1a) 3-methoxy-6-chloro-4-nitropyridazine 1-oxide (1b) or 3,6-dimethoxy-4-nitropyridazine 1-oxide (1c) with a solution of potassium permanganate in liquid ammonia gives in reasonable-to-good yields the corresponding 5-amino-4-nitropyridazine 1-oxides (75percent, 54percent and 62percent, respectively). 3,6-Dimethoxypyridazine (4a) and 3-methoxypyridazine (4b) are converted into the corresponding 4-aminopyridazines 6a,6b on treatment with potassium amide/liquid ammonia/potassium permanganate (yield 50 and 22percent respectively).In the last-mentioned reacti on besides 6b 3,3'-dimethoxy 4,4'-bipyridazine (7, 23percent) was obtained.It is suggested that the neutral 1:1 ?-adducts formed between (1a-1c) and liquid ammonia and the anionic ?-adducts, formed between (5a-5b) and potassium amide are intermediates in this amino-oxidation reaction.
