220168-41-2 Usage
Description
(Benzoyl-phenylmethoxy-amino) 4-methoxybenzoate is a versatile chemical compound belonging to the benzophenone derivatives. It features a benzoyl moiety and a 4-methoxybenzoate group, which contribute to its potential applications in various fields, including pharmaceuticals and organic synthesis.
Uses
Used in Pharmaceutical Industry:
(Benzoyl-phenylmethoxy-amino) 4-methoxybenzoate is used as a potential building block for the synthesis of more complex organic molecules, which could be utilized in the development of new pharmaceutical compounds.
Used in Cosmetics Industry:
(Benzoyl-phenylmethoxy-amino) 4-methoxybenzoate is used as a potential sunscreen agent due to its ability to absorb UV radiation, providing protection against harmful sun exposure and potentially reducing the risk of skin cancer.
Used in Antimicrobial Applications:
(Benzoyl-phenylmethoxy-amino) 4-methoxybenzoate is used as an antimicrobial agent, potentially offering protection against harmful microorganisms in various applications, such as in the medical or food industries.
Used in Antioxidant Applications:
(Benzoyl-phenylmethoxy-amino) 4-methoxybenzoate is used as an antioxidant, which could help prevent oxidative damage in various industrial processes or in the development of products that require protection against oxidation.
Overall, (benzoyl-phenylmethoxy-amino) 4-methoxybenzoate is a promising compound with potential applications in the pharmaceutical, cosmetics, antimicrobial, and antioxidant industries, among others. Its versatility and unique structure make it a valuable candidate for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 220168-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,6 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 220168-41:
(8*2)+(7*2)+(6*0)+(5*1)+(4*6)+(3*8)+(2*4)+(1*1)=92
92 % 10 = 2
So 220168-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H19NO5/c1-26-20-14-12-19(13-15-20)22(25)28-23(21(24)18-10-6-3-7-11-18)27-16-17-8-4-2-5-9-17/h2-15H,16H2,1H3
220168-41-2Relevant articles and documents
A comparison of the reactivity and mutagenicity of n-(benzoyloxy)-n-(benzyloxy)benzamides
Glover, Stephen A.,Hammond, Gerard P.,Bonin, Antonio M.
, p. 9684 - 9689 (2007/10/03)
A new series of N-(acyloxy)-N-alkoxybenzamides, AT-(benzoyloxy)-JV-(benzyloxy)benzamides 7 have been synthesized and have been found to be direct acting mutagens in Salmonella TA100. They undergo AAl1 solvolysis to give N-benzoyl-N-(benzyloxy)nitrenium ions 3 under conditions of acid catalysis as well as unusual BAl2 reactions at nitrogen with hydroxide. The latter process affords as intermediates the anomeric hydroxamic esters 4 which rearrange intramolecularly to esters in a HERON reaction. Rates of acid-catalyzed solvolysis and reaction with hydroxide ions correlate with Hammett σ values with low sensitivity (ρ = +0.32 and +0.55, respectively) in accordance with the AAl1 and BAl2 mechanisms. Mutagenicity for the series also appears to correlate with Hammett σ values but with low, negative sensitivity (p = -0.57), and their biological activity may be attributable to their stability under conditions of the Ames assay and hydrophobic binding to DNA, rather than their chemical reactivity.