1232407-68-9 Usage
Uses
Used in Pharmaceutical Research:
1-(2-Bromo-6-fluorophenyl)ethanol is used as a reagent in pharmaceutical research for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-Bromo-6-fluorophenyl)ethanol is used as a starting material for the preparation of other chemical derivatives. Its versatility and reactivity contribute to the synthesis of a wide range of organic compounds, including those with potential applications in various industries.
Used in Chiral Chemistry:
As a chiral molecule, 1-(2-Bromo-6-fluorophenyl)ethanol is used in chiral chemistry to study the properties and behavior of its enantiomers. This research is crucial for understanding the stereochemistry of molecules and their interactions with biological systems, which can lead to the development of more effective and selective drugs.
Used in Hazardous Substance Management:
Due to its potential to cause irritation to the skin, eyes, and respiratory system, 1-(2-Bromo-6-fluorophenyl)ethanol is also used in the development and implementation of safety protocols and guidelines for handling hazardous substances in laboratories and industrial settings. This ensures the protection of workers and the environment from potential harm.
Check Digit Verification of cas no
The CAS Registry Mumber 1232407-68-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,2,4,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1232407-68:
(9*1)+(8*2)+(7*3)+(6*2)+(5*4)+(4*0)+(3*7)+(2*6)+(1*8)=119
119 % 10 = 9
So 1232407-68-9 is a valid CAS Registry Number.
1232407-68-9Relevant academic research and scientific papers
The intramolecular reaction of acetophenoneN-tosylhydrazone and vinyl: Br?nsted acid-promoted cationic cyclization toward polysubstituted indenes
Wang, Zhixin,Li, Yang,Chen, Fan,Qian, Peng-Cheng,Cheng, Jiang
, p. 1810 - 1813 (2021/02/27)
In the presence of TsNHNH2, a Br?nsted acid-promoted intramolecular cyclization ofo-(1-arylvinyl) acetophenone derivatives was developed, leading to polysubstituted indenes with complexity and diversity in moderate to excellent yields. In sharp contrast with either the radical or carbene involved cyclization of aldehydicN-tosylhydrazone with vinyl, a cationic cyclization pathway was involved, whereN-tosylhydrazone served as an electrophile and alkylation reagent during this transformation.
