93796-59-9 Usage
Uses
Used in Pharmaceutical Industry:
Phenol, 3-bromo-5-methyl-4-nitro-, is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical sector, Phenol, 3-bromo-5-methyl-4-nitro-, serves as a building block for the creation of novel agrochemicals. Its properties make it suitable for the development of pesticides, herbicides, and other agricultural chemicals that can effectively control pests and enhance crop yields.
Used in Dye Industry:
Phenol, 3-bromo-5-methyl-4-nitro-, is employed in the production of dyes due to its ability to impart color to various substrates. Its chemical structure allows it to be used in the formulation of dyes for textiles, plastics, and other materials, offering a wide range of color options and improved dye performance.
Used in Materials Science:
Phenol, 3-bromo-5-methyl-4-nitro-, has potential applications in materials science, where its unique properties can be harnessed to develop new materials with specific characteristics. For instance, it can be used in the synthesis of polymers, coatings, and adhesives that exhibit enhanced properties such as improved thermal stability, chemical resistance, or mechanical strength.
Check Digit Verification of cas no
The CAS Registry Mumber 93796-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,9 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93796-59:
(7*9)+(6*3)+(5*7)+(4*9)+(3*6)+(2*5)+(1*9)=189
189 % 10 = 9
So 93796-59-9 is a valid CAS Registry Number.
93796-59-9Relevant academic research and scientific papers
Naturally Occurring Dibenzofurans. Part 5. Synthesis of Melacarpic Acid
Carvalho, Christopher F.,Sargent, Melvyn V.
, p. 1613 - 1620 (2007/10/02)
The total synthesis of the lichen dibenzofuran melacarpic acid (5) was achieved by intramolecular Ullman coupling of methyl 5-bromo-4-(2-bromo-5-methoxy-3-methylphenoxy)-6-heptyl-2-methoxybenzoate (48) or methyl 6-heptyl-5-iodo-4-(2-iodo-5-methoxy-3-methyl-4-nitrophenoxy)-2-methoxybenzoate (46) followed by appropriate transformations.
