906673-56-1 Usage
Description
1-(2-bromo-5-fluorophenyl)ethanol is a chemical compound characterized by the molecular formula C8H8BrFO. It presents as a colorless to pale yellow liquid and is recognized for its significant role as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 1-(2-bromo-5-fluorophenyl)ethanol is distinguished by its phenol ring, which features a fluorine and bromine substituent, along with an ethyl group attached to the hydroxyl group. Given its potential hazards, it is crucial to handle and store 1-(2-bromo-5-fluorophenyl)ethanol with caution.
Uses
Used in Pharmaceutical Industry:
1-(2-bromo-5-fluorophenyl)ethanol is used as an intermediate for the production of various pharmaceuticals. Its unique chemical structure contributes to the development of new drugs, particularly those with antibacterial and antifungal properties. 1-(2-bromo-5-fluorophenyl)ethanol's ability to be modified and incorporated into different drug formulations makes it a valuable asset in the pharmaceutical sector.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-bromo-5-fluorophenyl)ethanol is utilized as an intermediate for the synthesis of pesticides. Its inherent antibacterial and antifungal properties render it an effective component in the creation of pesticides designed to protect crops from a range of diseases and infestations. By enhancing the efficacy of these pesticides, 1-(2-bromo-5-fluorophenyl)ethanol contributes to improved agricultural productivity and crop protection.
Used in Chemical Research:
1-(2-bromo-5-fluorophenyl)ethanol is also employed in chemical research, where its unique structure and properties are studied for potential applications in various fields. Researchers may explore its reactivity, stability, and the possibility of creating new derivatives with specific functions or improved properties. 1-(2-bromo-5-fluorophenyl)ethanol's versatility in chemical synthesis makes it an important tool for advancing scientific knowledge and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 906673-56-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,6,7 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 906673-56:
(8*9)+(7*0)+(6*6)+(5*6)+(4*7)+(3*3)+(2*5)+(1*6)=191
191 % 10 = 1
So 906673-56-1 is a valid CAS Registry Number.
906673-56-1Relevant articles and documents
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.
Asymmetric Synthesis and Application of Chiral Spirosilabiindanes
Chang, Xin,Chen, Hong-Chao,Li, Chuan-Ying,Ma, Pei-Long,Wang, Peng
supporting information, p. 8937 - 8940 (2020/04/30)
Reported here is the development of a class of chiral spirosilabiindane scaffolds by Rh-catalyzed asymmetric double hydrosilation, for the first time. Enantiopure SPSiOL (spirosilabiindane diol), a new type of chiral building block for the preparation of various chiral ligands and catalysts, was readily prepared on greater than 10 gram scale using this protocol. The potential of this new spirosilabiindane scaffold in asymmetric catalysis was preliminarily demonstrated by development of the corresponding monodentate phosphoramidite ligands (SPSiPhos), which were used in both a Rh-catalyzed hydrogenation and a Pd-catalyzed intramolecular carboamination.
Synthesis of fluorenyl alcohols: Via cooperative palladium/norbornene catalysis
Casnati, Alessandra,Fontana, Marco,Motti, Elena,Della Ca, Nicola
, p. 6165 - 6173 (2019/07/04)
Herein, we report a novel catalytic synthesis of substituted 9H-fluoren-9-ols starting from aryl iodides and secondary ortho-bromobenzyl alcohols in the presence of palladium/norbornene as a catalytic system. The present protocol exhibits high functional
