132633-86-4 Usage
Uses
Used in Research Applications:
2,4-dibromoestra-1,3,5(10),6-tetraene-3,17-diol diacetate is used as a research compound for studying the effects of estrogen on biological systems. It aids in the exploration of estrogen's role in various physiological processes and its potential influence on health and disease.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,4-dibromoestra-1,3,5(10),6-tetraene-3,17-diol diacetate is used as a reference compound to assist in the development of new treatments and drugs related to hormone regulation. Its structural and functional similarities to natural estrogen make it a valuable tool in designing medications that target estrogen receptors for therapeutic purposes.
Used in Analytical Chemistry:
2,4-dibromoestra-1,3,5(10),6-tetraene-3,17-diol diacetate is employed as a reference standard in analytical chemistry. It helps in the calibration of instruments and the development of methods for the detection and quantification of estrogenic compounds in various samples, ensuring the accuracy and reliability of analytical results.
Check Digit Verification of cas no
The CAS Registry Mumber 132633-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,3 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132633-86:
(8*1)+(7*3)+(6*2)+(5*6)+(4*3)+(3*3)+(2*8)+(1*6)=114
114 % 10 = 4
So 132633-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H24Br2O4/c1-11(25)27-19-7-6-17-14-4-5-15-16(13(14)8-9-22(17,19)3)10-18(23)21(20(15)24)28-12(2)26/h4-5,10,13-14,17,19H,6-9H2,1-3H3/t13-,14+,17-,19?,22-/m0/s1
132633-86-4Relevant academic research and scientific papers
Szendi, Zsuzsanna,Dombi, Gyoergy,Vincze, Iren
, p. 392 - 394 (1991)
[2,4,6,7-3H4]Estradiol is used for the quantitative determination of estradiol receptors. The synthesis of 2,4-dibromoestra-1,3,5(10),6-tetraene-3,17β-diol 3,17-diacetate, the convenient precursor of [2,4,6,7-3 H4]estradiol, is described. 6-Alkoxy compounds were also prepared and investigated.
