75965-84-3 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Dimethoxy-naphthalene-1-carbaldehyde is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-Dimethoxy-naphthalene-1-carbaldehyde is employed as a precursor in the production of various agrochemicals, aiding in the creation of compounds that can be used in pest control and crop protection.
Used in Organic Synthesis:
2,4-Dimethoxy-naphthalene-1-carbaldehyde is utilized as a building block in organic synthesis, enabling the creation of a wide range of organic compounds for diverse applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 75965-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75965-84:
(7*7)+(6*5)+(5*9)+(4*6)+(3*5)+(2*8)+(1*4)=183
183 % 10 = 3
So 75965-84-3 is a valid CAS Registry Number.
75965-84-3Relevant academic research and scientific papers
Manganese(III)-Mediated Formylation of Aromatic Compounds in the Presence of Malonic Acid
Nishino, Hiroshi,Tsunoda, Katsunori,Kurosawa, Kazu
, p. 545 - 550 (2007/10/02)
The reaction of naphthlenes with malonic acid in the presence of manganese(III) acetate gives naphthalenecarbaldehydes and naphthalenecarboxylic acids.Similar reactions of anthracene, pyrene, and methoxybenzenes also yield formylated and carboxylated products.It was found that the formyl group introduced to the aromatic ring was not derived from carboxymethyl radical generated directly by the thermolysis of manganese(III) acetate, but from a dicarboxymethyl radical formed by the interaction of malonic acid and manganese(III) acetate.In addition, it was also found that the dicarboxymethyl radicals attacked the position of the highest electron density on the aromatic ring and that this formylation was effective when the ionization potential of the aromatic copound was lower than 7.8 eV.
