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5-BROMO-2-PHENOXYPYRIMIDINE, a pyrimidine derivative with the molecular formula C11H8BrN3O, is a chemical compound featuring a bromine atom and a phenoxy group attached to the pyrimidine ring. It is a white to off-white solid that is sparingly soluble in water but soluble in organic solvents. 5-BROMO-2-PHENOXYPYRIMIDINE has potential applications in the pharmaceutical and agricultural industries due to its ability to modify and enhance biological activity.

257280-25-4

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257280-25-4 Usage

Uses

Used in Pharmaceutical Industry:
5-BROMO-2-PHENOXYPYRIMIDINE is used as an intermediate in the synthesis of pharmaceuticals for its role in modifying and enhancing the biological activity of various compounds. It contributes to the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
5-BROMO-2-PHENOXYPYRIMIDINE is used as an intermediate in the synthesis of agrochemicals, where it serves as a building block for the production of various organic compounds. Its ability to modify biological activity makes it a valuable component in the development of effective agricultural chemicals.
Used as a Building Block in Organic Compounds Production:
5-BROMO-2-PHENOXYPYRIMIDINE is utilized as a building block in the production of various organic compounds, highlighting its versatility and importance in the synthesis of a wide range of chemical products. Its unique structure and properties make it a key component in the creation of diverse chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 257280-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,7,2,8 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 257280-25:
(8*2)+(7*5)+(6*7)+(5*2)+(4*8)+(3*0)+(2*2)+(1*5)=144
144 % 10 = 4
So 257280-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrN2O/c11-8-6-12-10(13-7-8)14-9-4-2-1-3-5-9/h1-7H

257280-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-BROMO-2-PHENOXYPYRIMIDINE

1.2 Other means of identification

Product number -
Other names 5-bromanyl-2-phenoxy-pyrimidine

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:257280-25-4 SDS

257280-25-4Relevant academic research and scientific papers

Method of preparing Quinoline-5,8-dione derivatives for TGase 2 inhibitor

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Paragraph 0377-0380, (2020/04/28)

I Is -5,8- of the quinoline, dione derivative compound. of Formula I, or a stereoisomer or a pharmaceutically acceptable salt thereof, wherein the compound of Formula, TGase 2 has, inhibitory effects TGase 2, and thus the pharmaceutical composition may be useful for preventing or treating disorders or diseases mediated by TGase 2 or inhibiting. (by machine translation)

HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF EPILEPSY

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Paragraph 0111; 0144, (2020/06/19)

The present invention provides a novel heterocyclic compound represented by Formula [I] and a salt thereof: wherein the symbols are as defined in the specification, which is useful for treating, preventing and/or diagnosing seizure and the like in disease involving epileptic seizure or convulsive seizure (including multiple drug resistant seizure, refractory seizure, acute symptomatic seizure, febrile seizure and status epilepticus), as well as a medical use therefor.

BTK INHIBITOR COMPOUNDS

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Page/Page column 30; 31, (2019/05/22)

The invention provides BTK Inhibitor compounds, pharmaceutically acceptable salts, pharmaceutical compositions thereof, and methods of using these compounds, salts, or compositions to treat autoimmune diseases such as Rheumatoid Arthritis.

Reversible covalent Bruton's tyrosine kinase inhibitor, pharmaceutical composition and application thereof

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Paragraph 0149-0151, (2019/12/02)

The invention discloses a reversible covalent Bruton's tyrosine kinase (BTK) inhibitor compound, a pharmaceutical composition and application of the compound and the pharmaceutical composition in preparation of drugs for treating diseases, disorders or symptoms benefitting from inhibition of Bruton's tyrosine kinase activity. The compound provided by the invention has strong in-vitro BTK kinase inhibition activity, and can be applied to treatment of diseases, disorders or symptoms, including B-cell lymphoma, autoimmune diseases, inflammatory diseases and the like, which benefit from inhibitionof Bruton's tyrosine kinase activity, alone or in combination with other drugs.

Quinoline-5,8-dione derivatives for TGase 2 inhibitor, and the pharmaceutical composition comprising the same

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Paragraph 0263-0266, (2019/10/29)

The present invention relates to a quinolin-5,8-dione derivative compound represented by chemical formula I, an optical isomer thereof or a pharmaceutically acceptable salt thereof. The compound represented by chemical formula I of the present invention has a TGase 2 inhibitory effect, and the pharmaceutical composition comprising the same can be usefully used for preventing or treating disorders or diseases mediated by TGase 2 or response to TGase 2 inhibition.COPYRIGHT KIPO 2020

Selective Bruton's tyrosine kinase inhibitor and application thereof

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Paragraph 0194-0196, (2018/06/04)

The invention discloses a selective Bruton's tyrosine kinase (BTK) inhibitor compound, a pharmaceutical composition, preparation and application thereof to preparation of medicines for treating diseases, disorders or symptoms obtained from inhibition of Bruton's tyrosine kinase activity. The compound disclosed by the invention has anti-proliferation and inhibition effects on tumor cell lines including A549, MINO, OCI-LY10, TMD-8 and the like, has good anti-tumor activity in tumor models including Mino subcutaneous xenoplastic transplantation and the like and can be applied to medicines for treating solid tumors or leukemia related to human or animal cell proliferation; the compound disclosed by the invention has relatively good pharmacokinetic performance and can be orally taken to treat the solid tumors or the leukemia related to the human or animal cell proliferation or autoimmune diseases; the compound disclosed by the invention has a low hERG channel blocking property.

MULTIHETEROARYL COMPOUNDS AS INHIBITORS OF H-PGDS AND THEIR USE FOR TREATING PROSTAGLANDIN D2 MEDIATED DISEASES

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Page/Page column 40, (2010/04/23)

Multiheteroaryl compounds, their preparation, pharmaceutical compositions comprising these compounds, and their pharmaceutical use in the prevention and treatment of prostaglandin D2 mediated diseases and conditions that may be modulated by the inhibition of hematopoietic prostaglandin D synthase (H-PGDS).

HETEROARYL ETHERS AND PROCESSES FOR THEIR PREPARATION

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Page/Page column 28, (2009/12/05)

The present invention relates to processes for the preparation of heteroaryl ethers. In some embodiments, the processes relate to cross coupling reactions between triazol-1-yloxy and triazol-1-yl heterocycles with aryl boronic acids. In a further aspect, this invention also relates to compounds that are useful for the treatment of oncological diseases or disorders, and for the treatment of inflammation.

Heteroaryl ethers by oxidative palladium catalysis of pyridotriazol-1-yloxy pyrimidines with arylboronic acids

Bardhan, Sujata,Wacharasindhu, Sumrit,Wan, Zhao-Kui,Mansour, Tarek S.

supporting information; experimental part, p. 2511 - 2514 (2009/10/18)

The oxidative palladium-catalyzed cross-coupling of pyrimidines containing pyridotriazol-1-yloxy (OPt) as either a urea or an amide functional group with arylboronic acids in the presence of Cs2CO3 in DME containing 0.6-1.0% H2

Hydrogen peroxide mediated formation of heteroaryl ethers from pyridotriazol-1-yloxy heterocycles and arylboronic acids

Bardhan, Sujata,Tabei, Keiko,Wan, Zhao-Kui,Mansour, Tarek S.

supporting information; experimental part, p. 5733 - 5736 (2009/12/06)

Pyridotriazol-1-yloxypyrimidine 3 reacts with arylboronic acids under palladium-free, Cs2CO3, (0.8%) H2O2, and DME conditions to produce heteroaryl ethers 4-16 in good yields comparable to the oxidative palladiu

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