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4-Methoxychrysene is a synthetic organic compound that serves as an intermediate in the synthesis of 4-Hydroxychrysene, a hydroxylated metabolite of Chrysene. It plays a significant role in the formation of estrogenic metabolites and is utilized in studying estrogen activity.

63020-59-7

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63020-59-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Methoxychrysene is used as an intermediate in the synthesis of 4-Hydroxychrysene for [application reason] in the pharmaceutical industry. 4-METHOXYCHRYSENE aids in the development of drugs targeting estrogen-related conditions and diseases.
Used in Research and Development:
In the field of research and development, 4-Methoxychrysene is used as a key component in the synthesis of 4-Hydroxychrysene, which is essential for studying estrogen activity. This helps scientists better understand the mechanisms of estrogen and develop potential therapeutic agents for related health issues.

Check Digit Verification of cas no

The CAS Registry Mumber 63020-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,2 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63020-59:
(7*6)+(6*3)+(5*0)+(4*2)+(3*0)+(2*5)+(1*9)=87
87 % 10 = 7
So 63020-59-7 is a valid CAS Registry Number.

63020-59-7Downstream Products

63020-59-7Relevant academic research and scientific papers

Photocyclization of o-Halostilbenes

Olsen, Robert J.,Pruett, Stephen R.

, p. 5457 - 5460 (2007/10/02)

The photocyclization reactions of several ortho-halogenated stilbene derivatives were examined under both oxidative conditions (iodine/cyclohexane) and basic conditions (sodium methoxide/methanol).The major products were those anticipated from photodehydrogenation and photodehydrohalogenation, respectively.In some cases photodebromination of the product occurred.Some regiochemical control in phenanthrene synthesis can be achieved as is illustrated by a synthesis of dehydroorchinol acetate.

Oxygen Sensitization of Electron Capture Response to Isomers of Polycyclic Aromatic Amines and Hydroxides

Campbell, J. A.,Grimsrud, E. P.,Hageman, L. R.

, p. 1335 - 1340 (2007/10/02)

The use of the oxygen-sensitized constant-current electron capture detector (ECD) with gas chromatography for analyte identification is extended by examining the responses of numerous polycyclic aromatic amines and hydroxides where an appropriate EC-enhancing chemical tag has been attached to the amino group or the hydroxy group has been methylated.For the majority of isomeric groups examined, measured response enhancements of the derivatives are sufficiently dependent on structural differences as to provide an additional means by which substitution isomers can be differentiated.The ion chemistry responsible for the EC and oxygen-sensitized responses also has been examined by the use of an atmospheric pressure ionization mass spectrometer (APIMS).

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