24590-01-0

Basic information

• Product Name: [2-(acetyloxy)-5-nitrophenyl]methanediyl diacetate
• CAS NO: 24590-01-0
• Molecular Formula: C₁₃H₁₃NO₈
• Molecular Weight: 311.2442
• Mol File: 24590-01-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 420°C at 760 mmHg
• Flash Point: 174.9°C
• Density: 1.359g/cm³
• Vapor Pressure: 2.9E-07mmHg at 25°C
• Refractive Index: 1.533
• CAS DataBase Reference: [2-(acetyloxy)-5-nitrophenyl]methanediyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(acetyloxy)-5-nitrophenyl]methanediyl diacetate(24590-01-0)
• EPA Substance Registry System: [2-(acetyloxy)-5-nitrophenyl]methanediyl diacetate(24590-01-0)

Safety Data

• Hazardous Substances Data: 24590-01-0(Hazardous Substances Data)

Usage

General Description

[2-(acetyloxy)-5-nitrophenyl]methanediyl diacetate is a chemical compound with the molecular formula C10H9NO6. It is a diacetate ester of 2-(acetyloxy)-5-nitrophenylmethane-1,1-diyldioxy diacetic acid and is used in organic synthesis. [2-(acetyloxy)-5-nitrophenyl]methanediyl diacetate is a yellow powder that is insoluble in water but soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, and it also has potential applications in the field of research and development.

Upstream product

• 100-02-7 4-nitro-phenol 
• 108-24-7 acetic anhydride 
• 97-51-8 5-Nitrosalicylaldehyde 
• 67141-99-5 acetic acid 2-methyl-4-nitrophenyl ester 

Downstream Products

• 402826-43-1 tert-butyl (3-formyl-4-hydroxyphenyl)carbamate 
• 578710-63-1 N,N'-ethylenebis(salicylideneiminato)iron(II) 
• 14167-18-1 salcomine 
• 1166842-07-4 C₂₆H₃₄N₄O₆ 
• 16358-44-4 2-hydroxy-5-acetamidobenzaldehyde 
• 97-51-8 5-Nitrosalicylaldehyde 
• 177496-78-5 2-acetoxy-5-nitrobenzaldehyde 
• 24590-02-1 5-Acetamido-2-acetoxy-benzaldiacetat 
• 784193-20-0 acetyloxy(2-acetyloxy-5-aminophenyl)methyl acetate 

Relevant articles and documents

Magnetic substance and magnetic substance manufacturing method

[object] A magnetization technique that enhances magnetic properties of an organic compound is provided without damaging properties of the organic compound or while maintaining the structure of the organic compound. [solution] The present disclosure is a method for manufacturing a magnetic substance composed of crystals of a magnetization target compound and an electron acceptor by combining the magnetization target compound with the electron acceptor; forming a solution by dissolving a mixture of the magnetization target compound and the electron acceptor in a solvent; maintaining the solution in a very low temperature state and allowing the solution to deposit the crystals of the magnetic target compound and the electron acceptor; and separating the crystals from the solvent.

IRON-SALEN COMPLEX

The present invention provides a drug delivery system that overcomes conventional technical problems and that is readily put to practical use. Iron-salen complexes represented by General Formula (I) below. The invention renders iron-salen complexes magnetic, which can thus be used as drugs that can be delivered to affected areas in the body using the inherent magnetic properties of the drug without employing carriers composed of magnetic substances as has been done hitherto.

Iron-salen complexes, magnetic drug, chemical induction system, and a magnetic detecting device

PROBLEM TO BE SOLVED: To realize, by solving technical problems of the prior art, a drug delivery system which can be easily implemented practically.SOLUTION: The provided iron-salen complex is expressed by the following formula (1). Since the iron-salen complex per se can potentially be magnetic, it becomes possible, in a case where the same is used as a pharmaceutical, to guide the pharmaceutical to an affected site inside a patient's body by taking advantage of the magnetic property borne by the pharmaceutical per se without using carriers consisting of magnets, as in the prior art.