68575-35-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(3,5-Dichlorophenyl)-2-Propanol is used as a chiral auxiliary in asymmetric synthesis for the production of pharmaceuticals. Its unique structure allows for the creation of enantiomerically pure compounds, which are essential in the development of effective and safe medications.
Used in Cancer Treatment:
2-(3,5-Dichlorophenyl)-2-Propanol is used as an antineoplastic agent in cancer treatment. It has demonstrated potential in inhibiting the growth and progression of various types of cancer, making it a promising candidate for further research and development in oncology.
Used in Pain Management:
2-(3,5-Dichlorophenyl)-2-Propanol is used as an anti-inflammatory and analgesic agent. Its ability to reduce inflammation and alleviate pain makes it a valuable component in the development of medications for pain management.
Safety Precautions:
It is important to handle 2-(3,5-Dichlorophenyl)-2-Propanol with caution, as it is considered harmful if swallowed or inhaled and can cause irritation to the skin and eyes. Proper safety measures should be taken during its production, use, and disposal to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 68575-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,7 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68575-35:
(7*6)+(6*8)+(5*5)+(4*7)+(3*5)+(2*3)+(1*5)=169
169 % 10 = 9
So 68575-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10Cl2O/c1-9(2,12)6-3-7(10)5-8(11)4-6/h3-5,12H,1-2H3
68575-35-9Relevant academic research and scientific papers
Direct α-Arylation of Alcohols with Aryl Halides through a Radical Chain Mechanism
Aoki, Kohei,Yonekura, Kyohei,Ikeda, Yuko,Ueno, Ryota,Shirakawa, Eiji
supporting information, p. 2200 - 2204 (2020/05/05)
Alcohols were found to be arylated directly at their α-C?H bond with aryl halides in the presence of a base and a substoichiometric amount of t-BuOOt-Bu through a homolytic aromatic substitution mechanism. (Figure presented.).
ARYL AND HETEROARYL ETHER COMPOUNDS AS ROR GAMMA MODULATORS
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Page/Page column 47; 48; 51, (2015/11/09)
The present disclosure is directed to compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein Ring A, Ring B, R, R2, R3, n, and p are as defined herein, which are active as modulators of retinoid-related orpha
