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6876-00-2

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6876-00-2 Usage

General Description

3-Phenoxybromobenzene is a chemical compound with the molecular formula C12H9BrO. It is a brominated arene compound with a phenoxy group attached to the benzene ring. 3-PHENOXYBROMOBENZENE is used in organic synthesis as a building block for the preparation of various plastics, pharmaceuticals, and agrochemicals. It is also used as an intermediate in the production of dyes, perfumes, and other industrial chemicals. It is a solid at room temperature and is insoluble in water but soluble in organic solvents. 3-Phenoxybromobenzene is classified as a hazardous chemical and should be handled with caution due to its potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 6876-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6876-00:
(6*6)+(5*8)+(4*7)+(3*6)+(2*0)+(1*0)=122
122 % 10 = 2
So 6876-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9BrO/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9H

6876-00-2SDS

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 3-Bromodiphenyl ether

1.2 Other means of identification

Product number -
Other names 1-bromo-3-phenoxybenzene

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:6876-00-2 SDS

6876-00-2Relevant articles and documents

BTK Inhibitors and uses thereof

-

Paragraph 1667-1672, (2020/05/02)

The invention discloses a bruton's tyrosine kinase (BTK) inhibitor and use thereof. Specifically, the invention provides heteroaromatic compounds or stereoisomers, geometrical isomers, tautomers, racemates, nitrogen oxides, hydrates, solvates, metabolites and pharmaceutically acceptable salts or prodrugs thereof, and pharmaceutical compositions containing the heteroaromatic compounds; the invention also discloses use of the heteroaromatic compounds or the pharmaceutical compositions containing the heteroaromatic compounds in preparation of medicines; the medicines can be used for treating autoimmune diseases, inflammatory diseases or proliferative diseases.

Anthracene compound, preparing method of anthracene compound and organic light-emitting device

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Paragraph 0121-0126, (2017/05/02)

The invention provides an anthracene compound. The anthracene compound has a structure in the formula (I), wherein Q is the C1-60 alkyl group or the C6-60 aryl group or the C5-60 condensed ring group or the C5-60 heterocyclic group; Ar is the C6-60 aryl group or the C5-60 condensed ring group or the C5-60 heterocyclic group; and Ar1 is H, the C1-60 alkyl group, the C1-60 alkoxy group, the C1-60 ether group, the C6-60 aryl group, the C6-60 condensed ring group, the C6-60 heterocyclic group and the C6-60 arylamine group. Compared with the prior art, the anthracene compound is connected with an aromatic compound through anthracene, and the Q, Ar and Ar1 groups are introduced, so that a device emits blue light after the organic compound is applied to the organic light-emitting device; and meanwhile, the means that the above groups are used for adjusting the light-emitting wavelength is adopted, the light-emitting efficiency of the organic light-emitting device is high, and the service life is long.

Visible-light-mediated synthesis of diaryl ethers from arylboronic acids and diaryliodonium salts

Liu, Li,Tang, Jiaqi,Qiang, Jian,Li, Jian,He, Mingyang

, p. 261 - 264 (2016/07/06)

With visible-light irradiation, a simple and metal-free photocatalytic system for the synthesis of diaryl ethers from arylboronic acids and diaryliodonium salts has been developed. The reaction proceeded in high yield for a range of different substrates in the presence of eosin Y under mild reaction conditions.

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