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2'-BROMO-4-FLUORO-BIPHENYL, with the molecular formula C12H8BrF, is a chemical compound that is a derivative of biphenyl. It features a bromine and a fluorine atom attached to the aromatic rings, giving it unique electronic and optical properties. 2'-BROMO-4-FLUORO-BIPHENYL is recognized for its potential applications in various fields, including pharmaceuticals, agrochemicals, materials science, and organic electronics.

89346-54-3

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89346-54-3 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2'-BROMO-4-FLUORO-BIPHENYL is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to be a key component in the development of new drugs and agricultural chemicals, enhancing their efficacy and performance.
Used in Organic Chemistry:
As a building block in organic chemistry, 2'-BROMO-4-FLUORO-BIPHENYL plays a crucial role in the synthesis of complex organic molecules. Its presence in these molecules can impart specific properties, making it valuable for research and development in the field of organic chemistry.
Used in Liquid Crystal and OLED Material Production:
2'-BROMO-4-FLUORO-BIPHENYL is employed in the production of liquid crystals and OLED (Organic Light Emitting Diode) materials. Its electronic and optical properties make it suitable for these applications, contributing to the advancement of display and lighting technologies.
Used in Materials Science and Organic Electronics:
Due to its unique electronic and optical properties, 2'-BROMO-4-FLUORO-BIPHENYL has potential applications in the field of materials science and organic electronics. It can be used to develop new materials with improved performance characteristics for use in electronic devices and other technologies.
Safety Precautions:
It is important to handle 2'-BROMO-4-FLUORO-BIPHENYL with care, as it can be harmful if ingested or inhaled. Additionally, it may cause skin and eye irritation upon contact, necessitating proper safety measures during its use and manipulation.

Check Digit Verification of cas no

The CAS Registry Mumber 89346-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,4 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89346-54:
(7*8)+(6*9)+(5*3)+(4*4)+(3*6)+(2*5)+(1*4)=173
173 % 10 = 3
So 89346-54-3 is a valid CAS Registry Number.

89346-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-(4-fluorophenyl)benzene

1.2 Other means of identification

Product number -
Other names 2-bromo-4'-fluorobiphenyl

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:89346-54-3 SDS

89346-54-3Relevant academic research and scientific papers

Rhodium-Catalyzed Synthesis of Chiral Monohydrosilanes by Intramolecular C?H Functionalization of Dihydrosilanes

Ma, Wenpeng,Liu, Li-Chuan,An, Kun,He, Tao,He, Wei

supporting information, p. 4245 - 4251 (2020/12/25)

The preparation of chiral monohydrosilanes remains a rarely achieved goal. To this end a Rh-catalyzed desymmetrization of dihydrosilanes by way of intramolecular C(sp2)?H functionalization under simple and mild conditions has now been developed

Further lead optimization on Bax activators: Design, synthesis and pharmacological evaluation of 2-fluoro-fluorene derivatives for the treatment of breast cancer

Liu, Gang,Kim, Hyejin,Wang, Pingyuan,Fricke, Doerte R.,Chen, Haiying,Wang, Tianzhi,Shen, Qiang,Zhou, Jia

, (2021/04/19)

To further pursue potent Bax activators with better safety profiles for the treatment of breast cancer, structural optimization was conducted based on lead compound CYD-4-61 through several strategies, including scaffold hopping on the 2-nitro-fluorene ring, replacement of the nitro group with bioisosteres to avoid potential toxicity, and further optimization on the upper pyridine by exploring diverse alkylamine linkers as a tail or replacing the pyridine with bioisosteric heterocycles. F-containing compound 22d (GL0388) exhibited a good balance between the activity and toxicity, displaying submicromolar activities against a variety of cancer cell lines with 5.8–10.7-fold selectivity of decreased activity to MCF-10A human mammary epithelial cell line. Compound 22d dose-dependently blocked colony formation of breast cancer cells and prevented the migration and invasion of MDA-MB-231 cells. Mechanism of action studies indicate that 22d activated Bax, rendering its insertion into mitochondrial membrane, thereby leading to cytochrome c release from the mitochondria into the cytoplasm, subsequently inducing release of apoptotic biomarkers. Further in vivo efficacy studies of 22d in human breast cancer xenografts arisen from MDA-MB-231 cells demonstrated that this drug candidate significantly suppressed tumor growth, indicating the therapeutic promise of this class of compounds for the treatment of breast cancer as well as the potential for developing F-radiolabeled imaging ligands as anticancer chemical probes.

Synthesis of Dibenzosiloles through Electrocatalytic Sila-Friedel-Crafts Reaction

Han, Pan,Yin, Mengyun,Li, Haiqiong,Yi, Jundan,Jing, Linhai,Wei, Bangguo

supporting information, p. 2757 - 2761 (2021/04/16)

A novel electrocatalyzed method for the preparation of dibenzosiloles was developed through intramolecular C?H/Si?H dehydrogenative coupling strategy starting from biarylhydrosilanes. Both electro-donating and electro-withdrawing substitution groups were tolerated for this transformation, and the desired dibenzosilole products could be obtained in moderate to excellent yields. A sila-Friedel-Crafts reaction mechanism was proposed on the basis of previous literature and our controlled experiments. (Figure presented.).

Palladium-catalyzed relay C–H functionalization to construct novel hybrid-arylcyclophosphorus ligand precursors

Bai, Peng-Bo,Wang, Juan,Yang, Shang-Dong

supporting information, (2021/11/17)

A new relay C–H functionalization of di([1,1′-biphenyl]-2-yl)phosphine oxide to obtain esterified and hydroxylated products with different hypervalent iodines as oxidants under palladium catalysis is disclosed. This reaction provides a more effective and concise strategy for the synthesis of novel structural hybrid-arylcyclophosphorus ligand precursors with a wide range of substrates and good functional group tolerance.

Ag-Catalyzed Cyclization of Arylboronic Acids with Elemental Selenium for the Synthesis of Selenaheterocycles

Gao, Wen-Xia,Huang, Xiao-Bo,Liu, Miao-Chang,Wu, Hua-Yue,Zhang, Xue,Zhou, Yun-Bing

supporting information, p. 5639 - 5644 (2020/11/30)

A general method for the synthesis of five-membered and six-membered selenaheterocycles through Ag-catalyzed C?Se bond-forming reaction is reported. This reaction proceeds via intramolecular cyclization of arylboronic acids with selenium powder. Preliminary mechanism studies demonstrate that this transformation involves a selenium-centred radical intermediate. (Figure presented.).

Visible-Light-Promoted, Catalyst-Free Gomberg-Bachmann Reaction: Synthesis of Biaryls

Lee, Juyoung,Hong, Boseok,Lee, Anna

, p. 9297 - 9306 (2019/08/12)

Biaryls were synthesized via a novel visible-light-promoted Gomberg-Bachmann reaction that does not require a photosensitizer or any metal reagents. The formation of an electron donor-acceptor complex between aryl diazonium salts and pyridine allows, under visible-light irradiation, the synthesis of biaryls in moderate-to-high yields.

Condensed fluorene derivative comprising heterocyclic ring

-

Paragraph 0397-0403, (2019/12/25)

The present invention relates to a condensed fluorene derivative comprising a heterocyclic ring and, more particularly, to an intermediate product for manufacturing a heterocyclic ring compound which can show excellent luminance and luminous efficiency when used as an organic light emitting material, while exhibiting excellent element characteristics with a long lifespan.COPYRIGHT KIPO 2020

Visible-Light Induced Radical Silylation for the Synthesis of Dibenzosiloles via Dehydrogenative Cyclization

Yang, Chao,Wang, Jing,Li, Jianhua,Ma, Wenchao,An, Kun,He, Wei,Jiang, Chao

supporting information, p. 3049 - 3054 (2018/08/06)

A visible-light induced radical silylation to dibenzosiloles from biarylhydrosilanes is described. The products were obtained in satisfactory yields under mild and water/air compatible conditions, providing an efficient and practical method for the synthesis of difunctionalized siloles by using a cheap organic dye photocatalyst. The method is tolerated by a wide range of functional groups and has a broad substrate scope. Light/dark experiments and quantum yield measurements provided support for a photocatalytic pathway rather than a chain process. (Figure presented.).

NOVEL INHIBITORS

-

Page/Page column 183, (2018/10/25)

The invention relates to a compound of formula (I): A-B-D-E (I) or a pharmaceutically acceptable salt, solvate or polymorph thereof, including all tautomers and stereoisomers thereof, wherein: A is selected from monocyclic and bicyclic heteroaryl, which may independently substituted by alkyl or amino; B is selected from alkyl, heteroalkyl, alkyl-amino, aryl, heteroaryl, cycloalkyl, heterocyclyl and alkylene, wherein said groups may independently be substituted by alkyl; D is selected from aryl-amino, heteroaryl-amino, cycloalkyl-amino, heterocyclyl, heterocyclyl-amino, urea, thioamide, thiourea, sulfonamide, sulfoximine and sulfamoyl, wherein said aryl, heteroaryl, cycloalkyl and heterocyclyl groups may independently be substituted; and E is selected from aryl, heteroaryl, cycloalkyl, heterocyclyl, wherein said aryl, heteroaryl, cycloalkyl and heterocyclyl groups may independently be substituted. The compounds of formula (I) are inhibitors of glutaminyl cyclase (QC, EC 2.3.2.5). QC catalyzes the intramolecular cyclization of N-terminal glutamine residues into pyroglutamic acid (5-oxo-prolyl, pGlu*) under liberation of ammonia and the intramolecular cyclization of N- terminal glutamate residues into pyroglutamic acid under liberation of water.

Construction of Chiral Tetraorganosilicons by Tandem Desymmetrization of Silacyclobutanes/Intermolecular Dehydrogenative Silylation

Zhang, Qing-Wei,An, Kun,Liu, Li-Chuan,Zhang, Qi,Guo, Huifang,He, Wei

supporting information, p. 1125 - 1129 (2017/01/18)

We report a method to construct chiral tetraorganosilicons by tandem silacyclobutane (SCB) desymmetrization–dehydrogenative silylations. A wide array of dibenzosiloles with stereogenic quaternary silicon centers were obtained in good yields and enantioselectivities up to 93 % ee. Chiral TMS-segphos was found to be a superior ligand in terms of reactivity and enantioselectivity.

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