21 Results for "

Fluoropyridines

" in MedChemExpress (MCE) Product Catalog:
Products (21)

21 Results for "Fluoropyridines" in MCE Product Catalog:

Cat. No.: HY-32742
CAS No.: 128071-98-7
4-Bromo-2-fluoropyridine is a drug intermediate .
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Cat. No.: HY-32951
CAS No.: 401815-98-3
2-Fluoropyridine-4-boronic acid is a coupling reagent and chemical intermediate. 2-Fluoropyridine-4-boronic acid facilitates the synthesis of Rho kinase (ROCK) inhibitor Compound 37 .
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Cat. No.: HY-W058423
CAS No.: 885267-36-7
6-Bromo-3-fluoropyridine-2-carbaldehyde (synthetic intermediate of Compound I-90) is a synthetic intermediate. 6-Bromo-3-fluoropyridine-2-carbaldehyde can be used in the synthesis of HPK1 inhibitors. 6-Bromo-3-fluoropyridine-2-carbaldehyde is applicable to research on immune diseases and hematological diseases .
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Cat. No.: HY-W012386
CAS No.: 444120-95-0
Synonyms: 6-Fluoropyridine-3-boronic acid pinacol ester
Research Areas:  

Others

2-Fluoropyridine-5-boronic acid pinacol ester is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-W003601
CAS No.: 357927-50-5
2-Bromo-4-fluoropyridine is a synthetic halogenated heterocyclic organic compound and a key intermediate in the pharmaceutical and agrochemical industries. 2-Bromo-4-fluoropyridine can be used to synthesize bioactive molecules through cross-coupling reactions, such as Suzuki coupling or Buchwald-Hartwig amination.
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Cat. No.: HY-Y0107
CAS No.: 21717-96-4
Target:  

Drug Intermediate

Research Areas:  

Others

2-Amino-5-fluoropyridine is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-32748
CAS No.: 41404-58-4
Research Areas:  

Others

2-Bromo-5-fluoropyridine acts as a bromofluoropyridine starting material and an azaaryl halide coupling partner. 2-Bromo-5-fluoropyridine participates in an oxygen-promoted, ligand-free Pd (OAc)2-catalyzed Suzuki reaction, reacting with arylboronic acids to produce 5-fluoro-2-aryl-substituted pyridine derivatives. 2-Bromo-5-fluoropyridine can be used to synthesize 5-fluoro-2-(4-(methylsulfonyl) phenyl) pyridine, an intermediate of the GPR119 agonist GSK1292263A .
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Cat. No.: HY-W003162
CAS No.: 1597-32-6
2-Amino-6-fluoropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-W010023
CAS No.: 869557-43-7
Synonyms: 3-Bromo-5-fluoro-2-pyridinamine
2-Amino-3-bromo-5-fluoropyridine (3-Bromo-5-fluoro-2-pyridinamine) is a drug intermediate that can be used for the synthesis fluorinated pyridines .
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Cat. No.: HY-W005118
CAS No.: 944401-77-8
Synonyms: 4-Fluoropyridin-2-amine
Target:  

Drug Intermediate

Research Areas:  

Others

2-Amino-4-fluoropyridine (4-Fluoropyridin-2-amine) is an intermediate. 2-Amino-4-fluoropyridine can be used in research on the synthesis of PKCζ inhibitors .
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Cat. No.: HY-32746
CAS No.: 766-11-0
Research Areas:  

Others

5-Bromo-2-fluoropyridine is a halogenated pyridine precursor. 5-Bromo-2-fluoropyridine participates in Li-Br exchange to generate a pyridyl zinc halide for Negishi cross-coupling in the synthesis of nicotinic acetylcholine receptor agonist analogues .
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Cat. No.: HY-P5372A
Research Areas:  

Cancer

Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2 TFA, a bioactive peptide, is a selective Protease activating receptor 1 (PAR-1) agonist over PAR-2. PAR-1 belongs to a subfamily of G-protein coupled receptors and is known to mediate the cellular effects of thrombin. In addition to its varied cellular effects of thrombin, PAR-1 has also been shown to coordinate with PAR-4 and regulate thrombin-induced hepatocellular carcinoma harboring thrombin formation within the tumor environment classified as 'coagulation type' .
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Cat. No.: HY-32952
CAS No.: 351019-18-6
Synonyms: 6-Fluoropyridine-3-boronic acid
Target:  

FAAH

2-Fluoropyridine-5-boronic acid (6-Fluoropyridine-3-boronic acid) is a fatty acid amide hydrolase (FAAH) inhibitor with an IC50 of 10 μM. 2-Fluoropyridine-5-boronic acid is applicable to research related to inflammation and pain .
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Cat. No.: HY-43727
CAS No.: 1187836-89-0
Research Areas:  

Others

6-Bromo-2-(bromomethyl)-3-fluoropyridine is a biological molecule.
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Cat. No.: HY-W002688
CAS No.: 82671-06-5
2,6-Dichloro-5-fluoropyridine-3-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2,6-Dichloro-5-fluoropyridine-3-carboxylic acid can be used in the synthesis of TAK-659 (HY-100867) .
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Cat. No.: HY-32950
CAS No.: 174669-73-9
2-Fluoropyridine-3-boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-65254
CAS No.: 1827-27-6
5-Amino-2-fluoropyridine is a fluorinated heterocyclic compound, which can be used for the synthesis of other active compounds .
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Cat. No.: HY-P5373
CAS No.: 237409-87-9
Target:  

Peptides

Research Areas:  

Others

Ser-parafluoroPhe-Aad-Leu-Arg-Asn-Pro-NH2 is a biological active peptide. (Structure-activity studies of thrombin receptor-tethered ligand SFLLRNP have revealed the importance of the Phe-2-phenyl group in receptor recognition and the replacement of the Phe-2 by para-fluorophenylalanine [(p-F)Phe] was found to enhance its activity)
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Cat. No.: HY-P5372
CAS No.: 211190-38-4
Research Areas:  

Cancer

Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2, a bioactive peptide, is a selective Protease activating receptor 1 (PAR-1) agonist over PAR-2. PAR-1 belongs to a subfamily of G-protein coupled receptors and is known to mediate the cellular effects of thrombin. In addition to its varied cellular effects of thrombin, PAR-1 has also been shown to coordinate with PAR-4 and regulate thrombin-induced hepatocellular carcinoma harboring thrombin formation within the tumor environment classified as 'coagulation type' .
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Cat. No.: HY-W005596
CAS No.: 669066-91-5
Synonyms: 5-Bromo-3-fluoropyridine-2-carboxylic acid
5-Bromo-3-fluoropicolinic acid (5-Bromo-3-fluoropyridine-2-carboxylic acid) is a drug synthesis intermediate that can be used to synthesize an inhibitor of glycinamide ribonucleotide formyltransferase .
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