72323-93-4 Usage
General Description
4-Benzyloxy-3-methylbenzoic acid is a chemical compound with the molecular formula C15H14O3. It is a white to off-white solid that is sparingly soluble in water. The compound is often used as a building block in organic synthesis, particularly in the production of pharmaceuticals and other fine chemicals. It is also used as a precursor to various other chemical compounds. In addition, 4-benzyloxy-3-methylbenzoic acid has been studied for its potential antioxidant and anti-inflammatory properties, making it of interest for use in various medical and cosmetic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 72323-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,2 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72323-93:
(7*7)+(6*2)+(5*3)+(4*2)+(3*3)+(2*9)+(1*3)=114
114 % 10 = 4
So 72323-93-4 is a valid CAS Registry Number.
72323-93-4Relevant articles and documents
RADIOHALOGEN PROSTHETIC MOIETIES AND RADIOLABELED BIOMOLECULES
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Page/Page column 23, (2021/05/21)
The application is drawn to radiohalogen prosthetic moieties and precursors thereof and to radiolabeled biomolecules comprising such radiohalogen prosthetic moieties. The biomolecules have an affinity for particular types of cells and may specifically bind a certain cell, such as a cancer cell. Relevant biomolecules include antibodies, monoclonal antibodies, antibody fragments, peptides, other proteins, nanoparticles, aptamers, and pharamacological moieties used to target prostate-specific membrane antigen (PSMA).
LOW MELTING NEMATIC DERIVATIVES OF PHENYL 3-METHYL-BENZOYLOXYBENZOATE.
Young,Green
, p. 7 - 9 (2007/10/13)
A series of forty-eight low melting nematogenic dialkyl derivatives of type R**3 equals CH//3 (R**1 and R**2 are n-alkyls) are presented, one of which melts to the nematic phase at 43 C. The compounds were prepared by a six-step procedure with an average yield per step of 90%.
