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3-(4-Fluorobenzyloxy)-bromobenzene, with the molecular formula C13H10BrFO, is a brominated aromatic compound featuring a fluorobenzyloxy side chain. This versatile chemical is recognized for its unique structure and properties, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its utility extends to organic synthesis and as a precursor for more complex compounds, as well as serving as a reagent in chemical reactions and a research tool in organic chemistry.

845866-52-6

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845866-52-6 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-Fluorobenzyloxy)-bromobenzene is used as a building block for the development of new pharmaceuticals due to its unique structure that can be further modified to create a variety of medicinal compounds. Its presence in the synthesis process can contribute to the discovery of novel drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(4-Fluorobenzyloxy)-bromobenzene is utilized as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the creation of compounds that can effectively control pests and weeds, thereby enhancing crop protection and yield.
Used in Specialty Chemicals Production:
3-(4-Fluorobenzyloxy)-bromobenzene is employed as a key component in the production of specialty chemicals, which are used in various industries such as plastics, coatings, and fragrances. Its unique characteristics enable the creation of high-performance materials with specific properties tailored to the needs of these industries.
Used as a Reagent in Chemical Reactions:
3-(4-FLUOROBENZYLOXY)-BROMOBENZENE serves as a reagent in a variety of chemical reactions, facilitating the synthesis of other complex organic compounds. Its reactivity and stability make it a reliable choice for researchers and chemists working on the development of new chemical entities.
Used as a Research Tool in Organic Chemistry:
3-(4-Fluorobenzyloxy)-bromobenzene is also used as a research tool in the field of organic chemistry, aiding scientists in understanding reaction mechanisms, exploring new synthetic routes, and advancing the knowledge of organic compounds and their applications.

Check Digit Verification of cas no

The CAS Registry Mumber 845866-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,8,6 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 845866-52:
(8*8)+(7*4)+(6*5)+(5*8)+(4*6)+(3*6)+(2*5)+(1*2)=216
216 % 10 = 6
So 845866-52-6 is a valid CAS Registry Number.

845866-52-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-3-[(4-fluorophenyl)methoxy]benzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:845866-52-6 SDS

845866-52-6Downstream Products

845866-52-6Relevant academic research and scientific papers

Synthesis and evaluation of small molecules bearing a benzyloxy substituent as novel and potent monoamine oxidase inhibitors

Lan, Jin-Shuai,Zhang, Tong,Liu, Yun,Zhang, Yong,Hou, Jian-wei,Xie, Sai-Sai,Yang, Jing,Ding, Yue,Cai, Zhen-zhen

, p. 471 - 478 (2017)

A new series of small molecules bearing a benzyloxy substituent have been designed, synthesized and evaluated for hMAO inhibitory activity in vitro. Most of the compounds were potent and selective MAO-B inhibitors, and were weak inhibitors of MAO-A. In particular, compounds 9e (IC50 = 0.35 μM) and 10e (IC50 = 0.19 μM) were the most potent MAO-B inhibitors, and exhibited the highest selectivity for MAO-B (9e, SI > 285.7-fold and 10e, SI = 146.8-fold). In addition, the structure-activity relationships for MAO-B inhibition indicated that electron-withdrawing groups in the open small molecules were more suitable for MAO-B inhibition, and substitutions at the benzyloxy of the open small molecules, particularly with the halogen substituted benzyloxy, were more favorable for MAO-B inhibition. Molecular docking studies have been done to explain the potent MAO-B inhibition of the open small molecules. Furthermore, the representative compounds 9e and 10e showed low neurotoxicity in SH-SY5Y cells in vitro. So the small molecules bearing the benzyloxy substituent could be used to develop promising drug candidates for the therapy of neurodegenerative diseases.

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