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Meso-3,3'-Dihydroxyhexestrol is a synthetic estrogen compound that belongs to the family of hexestrol derivatives. It is structurally similar to natural estrogens and exhibits potent estrogenic activity. This chemical is primarily used in pharmaceutical applications, particularly in the treatment of hormone-related conditions such as breast cancer and prostate cancer. Meso-3,3'-Dihydroxyhexestrol works by binding to estrogen receptors, thereby modulating the expression of genes involved in cell growth and differentiation. Due to its strong estrogenic effects, it is also used in veterinary medicine for the treatment of hormonal imbalances in animals. However, it is important to note that the use of this chemical is regulated due to potential side effects and health risks associated with long-term exposure to synthetic estrogens.

6052-94-4

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6052-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6052-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6052-94:
(6*6)+(5*0)+(4*5)+(3*2)+(2*9)+(1*4)=84
84 % 10 = 4
So 6052-94-4 is a valid CAS Registry Number.

6052-94-4Downstream Products

6052-94-4Relevant academic research and scientific papers

Ring-Substituted 1,2-Dialkylated 1,2-Bis(hydroxyphenyl)ethanes. 1. Synthesis and Estrogen Receptor Binding Affinity of 2,2'-and 3,3'-Disubstituted Hexestrols

Hartmann, Rolf W.,Schwarz, Walter,Schoenenberger, Helmut

, p. 1137 - 1144 (2007/10/02)

The syntheses of symmetrically 3,3'- and 2,2'-disubstituted meso hexestrol derivatives are described 3,3'-substituents: OH (1), F (2), Cl (3), Br (4), I (5), CH2N(CH3)2 (6), CH3 (7), CH2OCH3 (8), CH2OC2H5 (9), CH2OH (10), NO2 (11), NH2 (12) N(CH3)2 (13),

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