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2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER is a synthetic chemical compound characterized by the presence of a bromine atom, a nitro group, and a trifluoromethyl group attached to a diphenyl ether structure. This complex molecule exhibits unique properties due to its functional groups, which may lead to high reactivity under certain conditions. The trifluoromethyl group influences the compound's physical properties, such as volatility and stability, as well as its chemical properties, including reactivity and acidity. The ether linkage in the molecule suggests potential reactivity with a variety of organic and inorganic substrates, making it a versatile chemical for diverse applications. 2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER's potential to form numerous derivatives further enhances its utility in various industries and pharmaceuticals. Safe handling of 2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER requires a thorough understanding of its molecular structure and potential interactions in different conditions.

2069-14-9

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2069-14-9 Usage

Uses

Used in Chemical Synthesis:
2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER is used as a synthetic intermediate for the production of various chemical compounds. Its unique functional groups allow for further reactions and modifications, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER is used as a key component in the development of new drugs. Its potential reactivity with biological targets and ability to form derivatives make it a promising candidate for the creation of novel therapeutic agents.
Used in Material Science:
2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER is used as a component in the development of advanced materials, such as polymers and coatings, due to its potential to influence the properties of these materials. Its reactivity and the presence of the trifluoromethyl group can contribute to the creation of materials with improved stability, durability, and other desirable characteristics.
Used in Research and Development:
In research and development settings, 2-BROMO-2'-NITRO-4'-(TRIFLUOROMETHYL)DIPHENYL ETHER is used as a model compound to study the effects of its functional groups on chemical reactivity and interactions with other molecules. This can lead to a better understanding of the underlying chemistry and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 2069-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2069-14:
(6*2)+(5*0)+(4*6)+(3*9)+(2*1)+(1*4)=69
69 % 10 = 9
So 2069-14-9 is a valid CAS Registry Number.

2069-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-2'-nitro-4'-(trifluoromethyl)diphenyl ether

1.2 Other means of identification

Product number -
Other names 1-(2-bromophenoxy)-2-nitro-4-(trifluoromethyl)benzene

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:2069-14-9 SDS

2069-14-9Relevant articles and documents

Phenoxazine: A privileged scaffold for radical-trapping antioxidants

Farmer, Luke A.,Haidasz, Evan A.,Griesser, Markus,Pratt, Derek A.

, p. 10523 - 10536 (2018/05/31)

Diphenylamines are widely used to protect petroleum-derived products from autoxidation. Their efficacy as radical-trapping antioxidants (RTAs) relies on a balance of fast H-atom transfer kinetics and stability to one-electron oxidation by peroxidic specie

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