Fluorobenzenes

Organic compounds considered aryl halides that consist of a phenyl group with a fluorine atom substitution in the following structure: C₆H₅F.

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3,826 – 3,840 of 4,402 results

3,826

eMolecules 1177559-63-5 | (3-Bromo-2-fluorophenyl)methanamine hydrochloride | Apollo Scientific | MFCD13194195 | 240.500 | C7H8BrClFN | 95.000 | Cl.NCc1cccc(Br)c1F | 250mg | 562465498

(3-Bromo-2-fluorophenyl)methanamine hydrochloride | Apollo Scientific | 1177559-63-5 | MFCD13194195 | 240.500 | C7H8BrClFN | 95.000 | Cl.NCc1cccc(Br)c1F | 250mg | 562465498

Pricing & Availability

3,827

eMolecules 1005168-10-4 | Medchem Express | Asivatrep | 1mg | 446261777 | HY-12777 | MFCD28502100 | 491.48 | C21H22F5N3O3S

Pharmablock | benzyl (3R)-3-hydroxypiperidine-1-carboxylate | 250mg | 551058972 | PB00793 | 100858-34-2 | MFCD11112280 | 235.283 | C13H17NO3

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3,828

Medchemexpress LLC HY-107145 5mg Medchemexpress, Ningetinib Tosylate CAS:1394820-77-9 Purity:>98%

Medchemexpress, HY-107145 5mg Ningetinib Tosylate CAS:1394820-77-9 Ningetinib Tosylate is a potent, orally bioavailable small molecule tyrosine kinase inhibitor (TKI) with IC50s of 6.7, 1.9 and <1.0 nM for c-Met, VEGFR2 and Axl, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.

Pricing & Availability

3,829

Medchemexpress LLC 3-amino-4-{(3S)-3-[(2-ethoxyethoxy)methyl]piperidin-1-yl}thieno[2,3-b]pyridine-2-carboxamide | 2871872-79-4 | 99.9% | 378.49 | C18H26N4O3S | 5 MG

DS96432529 is a small-molecule cyclin-dependent kinase 8 (CDK8) inhibitor reported to have potent, orally active bone anabolic effects. It is supplied for research use and is characterized by a molecular formula of C18H26N4O3S, a molecular weight of 378.49 g/mol, and a CAS number of 2871872-79-4. Analytical documentation and a certificate of analysis are available.

Potent CDK8 inhibition with bone anabolic activity.
Orally active pharmacological profile in reported studies.
High purity (99.9%) suitable for research applications.
Available in small research pack sizes, including 5 mg.
Characterized by formula C18H26N4O3S and molecular weight 378.49 g/mol.
Analytical documentation available (COA, H NMR, LC-MS).

Pricing & Availability

3,830

eMolecules 121247-01-6 | 2-(3-Fluorophenyl)-2-oxoacetaldehyde | Synthonix - Stock | MFCD13151984 | 152.124 | C8H5FO2 | 95.000 | Fc1cccc(c1)C(=O)C=O | 1g | 495868646

2-(3-Fluorophenyl)-2-oxoacetaldehyde | Synthonix - Stock | 121247-01-6 | MFCD13151984 | 152.124 | C8H5FO2 | 95.000 | Fc1cccc(c1)C(=O)C=O | 1g | 495868646

Pricing & Availability

3,831

Medchemexpress LLC 1-[4-chloro-2-hydroxy-3-(3S-methyloxolan-3-yl)sulfonylphenyl]-3-(1R-2-methylcyclopentenyl)urea | 1838123-21-9 | 99.5% | 25 MG

CXCR2-IN-2 is a selective, brain-penetrant, orally bioavailable antagonist of the chemokine receptor CXCR2 used in preclinical pharmacology to probe CXCR2-mediated signaling and inflammatory responses. It demonstrates low-nanomolar potency in cell-based assays and high selectivity over related chemokine receptors.

Selective, brain-penetrant CXCR2 antagonist.
Low-nanomolar potency (IC50 5.2 nM in β-arrestin assay; 1 nM in CXCR2 Tango assay).
Inhibits Gro-α-induced CD11b expression in human whole blood (IC50 0.04 μM).
High selectivity versus CXCR1 and other chemokine receptors.
High purity (≈99.5%) and white to off-white solid appearance.
Soluble in DMSO (240 mg/mL); store powder at -20°C for long-term stability.
Offered as a 25 MG solid package suitable for preclinical studies.