35122-79-3 Usage
Uses
Used in Research and Development:
4-Chloro-2-methoxy-N-methylaniline 96% is used as a chemical intermediate for the synthesis of various organic compounds in research and development settings. Its unique structure allows it to undergo reactions that can lead to the creation of new molecules with potential applications in different industries.
Used in Chemical Synthesis Industry:
In the chemical synthesis industry, 4-Chloro-2-methoxy-N-methylaniline 96% is used as a key reactant in the production of specialty chemicals, pharmaceuticals, and agrochemicals. Its ability to participate in various chemical reactions makes it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
4-Chloro-2-methoxy-N-methylaniline 96% is used as a building block in the development of new pharmaceutical compounds. Its unique structure can be modified through chemical reactions to create potential drug candidates with novel therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Chloro-2-methoxy-N-methylaniline 96% is used as a precursor in the synthesis of new pesticides and herbicides. Its reactivity and structural features make it suitable for the development of effective and targeted agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 35122-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,2 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35122-79:
(7*3)+(6*5)+(5*1)+(4*2)+(3*2)+(2*7)+(1*9)=93
93 % 10 = 3
So 35122-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO/c1-10-7-4-3-6(9)5-8(7)11-2/h3-5,10H,1-2H3
35122-79-3Relevant academic research and scientific papers
Palladium-catalyzed N-nitroso-directed C-H alkoxylation of arenes and subsequent formation of 2-alkoxy-N-alkylarylamines
Gao, Tingting,Sun, Peipei
, p. 9888 - 9893 (2015/02/19)
(Chemical Equation Presented) A palladium-catalyzed direct ortho-alkoxylation of N-alkyl-N-nitrosoarylamines was developed in which alcohols were used as the alkoxylation reagents and PhI(OAc)2 was employed as the oxidant. The protocol was available for both primary and secondary alcohols. The products were transformed to o-alkoxy-N-alkylanilines expediently by a simple reduction.
