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The chemical compound "10,11,12,13-Tetrahydro-1,7-dihydroxy-10,13-dimethyldifuro[2',3':5,6:3'',2'':7,8]perylo[1,12-def][1,3]dioxepin-8,15-dione" is a complex organic molecule with a unique structure. It is characterized by a tetrahydro (four hydrogen atoms attached to a carbon ring) and dihydroxy (two hydroxyl groups) framework, which contributes to its stability and reactivity. The presence of two methyl groups at positions 10 and 13 adds to its complexity. The compound also features a difurano (two furan rings) and a perylene (a large aromatic system) structure, which are fused together in a specific arrangement. The numbering of the carbon atoms and the positions of the functional groups are crucial for understanding the molecule's properties and potential applications. 10,11,12,13-Tetrahydro-1,7-dihydroxy-10,13-dimethyldifuro[2',3':5,6:3'',2'':7,8]perylo[1,12-def][1,3]dioxepin-8,15-dione is likely to be of interest in the field of organic chemistry, particularly in the synthesis of complex heterocyclic compounds and may have applications in materials science or pharmaceuticals due to its intricate structure.

39657-83-5

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39657-83-5 Usage

Chemical structure

The compound has a complex structure consisting of a perylenequinone core, two fused dioxepin rings, a furan ring, and two hydroxyl groups.

Biological activity

The compound has potential biological activity and has been studied for its anti-tumor and anti-inflammatory properties.

DNA binding

The compound is known for its ability to bind to DNA, which may contribute to its biological activity.

Enzyme inhibition

The compound has been shown to inhibit the activity of certain enzymes, which may also contribute to its biological activity.

Medicinal chemistry

The compound represents an interesting scaffold for the development of new pharmaceuticals and has been the subject of research in the field of medicinal chemistry.

Molecular weight

The molecular weight of the compound is approximately 470.43 g/mol.

Solubility

The compound is likely to be soluble in organic solvents such as dimethyl sulfoxide (DMSO) and may have limited solubility in water.

Stability

The compound may be sensitive to light, heat, and moisture, and should be stored under appropriate conditions to maintain its stability.

Synthesis

The compound can be synthesized through various chemical reactions, including condensation, cyclization, and oxidation reactions.

Analytical techniques

The compound can be characterized and analyzed using techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and high-performance liquid chromatography (HPLC).

Safety precautions

As with any chemical compound, appropriate safety precautions should be taken when handling and working with 10,11,12,13-Tetrahydro-1,7-dihydroxy-10,13-dimethyldifuro[2',3':5,6:3'',2'':7,8]perylo[1,12-def][1,3]dioxepin-8,15-dione, including the use of personal protective equipment (PPE) and working in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 39657-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,5 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39657-83:
(7*3)+(6*9)+(5*6)+(4*5)+(3*7)+(2*8)+(1*3)=165
165 % 10 = 5
So 39657-83-5 is a valid CAS Registry Number.

39657-83-5Downstream Products

39657-83-5Relevant academic research and scientific papers

STEREOCHEMISTRY OF CERCOSPORIN

Nasini, Gianluca,Merlini, Lucio,Andreetti, Giovanni Dario,Bocelli, Gabriele,Sgarabotto, Paolo

, p. 2787 - 2796 (2007/10/02)

The absolute configuration of the asymmetric carbons and the axial chirality of the natural mold metabolite cercosporin (from Cercospora sp.) have been established on the basis of X-ray analysis and chemical reactions.The results confirm the inherent dissymetry of the perylenequinone ring, the twisting of which gives rise to the diastereoisomer isocercosporin.The energy barrier for the conversion of cercosporin into isocercosporin has been evaluated.

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