68266-27-3 Usage
Uses
Used in Industrial Processes:
Phenol,3,3'-(1,2-dibutyl-1,2-ethanediyl)bis(9CI) is used as a solvent in various industrial processes. Its unique chemical structure allows it to dissolve a wide range of substances, making it a valuable component in the production of various materials.
Used in Pharmaceutical Production:
This phenol derivative is also utilized in the production of pharmaceuticals. Its properties enable it to act as a key intermediate in the synthesis of certain drugs, contributing to the development of new medications.
Used in Organic Synthesis:
Phenol,3,3'-(1,2-dibutyl-1,2-ethanediyl)bis(9CI) is employed in the field of organic synthesis, where it serves as a building block for the creation of more complex organic compounds. Its versatility in forming chemical bonds with other molecules makes it a useful tool in the synthesis of a variety of organic products.
Used in Materials Science:
In the realm of materials science, Phenol,3,3'-(1,2-dibutyl-1,2-ethanediyl)bis(9CI) may have applications in the development of new materials with specific properties. Its unique structure could contribute to the creation of materials with enhanced characteristics, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 68266-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,6 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68266-27:
(7*6)+(6*8)+(5*2)+(4*6)+(3*6)+(2*2)+(1*7)=153
153 % 10 = 3
So 68266-27-3 is a valid CAS Registry Number.
68266-27-3Relevant academic research and scientific papers
Potential Antiestrogens. Synthesis and Evaluation of Mammary Tumor Inhibiting Activity of 1,2-Dialkyl-1,2-bis(3'-hydroxyphenyl)ethanes
Hartmann, Rolf W.,Buchborn, Helga,Kranzfelder, Gerhard,Schoenenberger, Helmut,Bogden, Arthur
, p. 1192 - 1197 (2007/10/02)
The syntheses of the meso-1,2-dialkyl-1,2-bis(3'-hydroxyphenyl)ethanes and of d,l-3,4-bis(3'-hydroxyphenyl)hexane (21) are described.In vitro these compounds inhibited the estradiol receptor interaction competitively, exhibiting Ka values between 0.20*109 (20) and 0.11*106 M-1 (24).In vivo the meso compounds reduced the estrone-stimulated mouse uterine growth; the most effective compounds were 20, 22, and 23 (53, 50, and 45percent inhibition, respectively).Compounds 20 and 22-24 showed weak estrogenic activity in the mouse uterine weight test and in the vaginal cornification test.Compounds 19 (NSC-297169), 20 (NSC-297170), and 22 (NSC-297171) exhibited a dose-dependent growth inhibition on the MCF-7 human breast tumor cell line (10-6 to 10-9 M).These compounds also showed a marked dose-dependent inhibition on the DMBA-induced, hormone-dependent mammary carcinoma of the Sprague-Dawley rat corresponding to their association constants.
Novel di-(3'-hydroxyphenyl)-alkane compounds, process of preparation and their use in medicine
-
, (2008/06/13)
Compounds of di-(3'-hydroxyphenyl)-alkanes and their methyl ethers, of the formula STR1 wherein R is alkyl and R' is H or methyl, have activity against hormone-dependent breast carcinoma.
