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130046-78-5

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130046-78-5 Usage

Description

2-(benzyloxy)-1,3-dibromo-5-fluorobenzene is a halogenated aromatic chemical compound with the molecular formula C14H10Br2F-O. It features a benzene ring with two bromine atoms at the 1 and 3 positions, a fluorine atom at the 5 position, and a benzyloxy group attached to the 2 position. 2-(benzyloxy)-1,3-dibromo-5-fluorobenzene is characterized by its specific reactivity and interactions with other compounds, making it a valuable starting material or reagent in organic synthesis and medicinal chemistry for the preparation of more complex molecules.

Uses

Used in Organic Synthesis:
2-(benzyloxy)-1,3-dibromo-5-fluorobenzene is used as a starting material or reagent in organic synthesis for the preparation of more complex molecules. Its unique structure and reactivity allow for various chemical reactions, enabling the synthesis of a wide range of compounds with diverse applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(benzyloxy)-1,3-dibromo-5-fluorobenzene serves as a building block for the development of new pharmaceutical compounds. Its specific functional groups and halogenated nature can be utilized to create molecules with potential therapeutic properties, such as antimicrobial, antiviral, or anticancer agents.
Used in Chemical Research:
2-(benzyloxy)-1,3-dibromo-5-fluorobenzene is also used in chemical research to study the reactivity and properties of halogenated aromatic compounds. Researchers can explore its potential applications in various chemical reactions and investigate its interactions with other compounds to gain insights into its behavior and possible uses.
Used in Specialty Chemicals Industry:
2-(benzyloxy)-1,3-dibromo-5-fluorobenzene can be employed in the specialty chemicals industry for the production of high-value compounds with specific applications. Its unique structure and reactivity make it suitable for the development of specialty chemicals used in various industries, such as pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 130046-78-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,4 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130046-78:
(8*1)+(7*3)+(6*0)+(5*0)+(4*4)+(3*6)+(2*7)+(1*8)=85
85 % 10 = 5
So 130046-78-5 is a valid CAS Registry Number.

130046-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Benzyloxy)-1,3-dibromo-5-fluorobenzene

1.2 Other means of identification

Product number -
Other names (2,6-Dibromo-4-fluoro-phenyl) benzyl ether

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:130046-78-5 SDS

130046-78-5Downstream Products

130046-78-5Relevant articles and documents

Phenylpiperazine derivatives with a combination of partial dopamine-D2 receptor agonism and serotonin reuptake inhibition

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Page/Page column 10, (2010/11/08)

The invention relates to a group of novel phenylpiperazine derivatives with a dual mode of action: serotonin reuptake inhibition and partial agonism on dopamine-D2 receptors. The invention also relates to the use of a compound disclosed herein for the manufacture of a medicament giving a beneficial effect. The compounds have the general formula (1): wherein the symbols have the meanings given in the specification. and tautomers, stereoisomers and N-oxides thereof, as well as pharmacologically acceptable salts, hydrates and solvates of said compounds of formula (1) and its tautomers, stereoisomers and N-oxides.

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