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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4,006 – 4,020 of 4,391 results

4,006

eMolecules 55660-73-6 | 2-Fluorobenzene-1,4-diol | Combi-Blocks | MFCD00061106 | 128.102 | C6H5FO2 | 95.000 | Oc1ccc(O)c(F)c1 | 1g | 517031940

2-Fluorobenzene-1,4-diol | Combi-Blocks | 55660-73-6 | MFCD00061106 | 128.102 | C6H5FO2 | 95.000 | Oc1ccc(O)c(F)c1 | 1g | 517031940

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4,007

Medchemexpress LLC Platicodigenin | 22327-82-8 | 520.70 | 5 MG

Platicodigenin is a compound isolated from the plant *Platycodon grandiflorum*.

Isolated from *Platycodon grandiflorum*

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4,008

Medchemexpress LLC Nucc-390 dihydrochloride | 2749281-71-6 | MFCD32690075 | 98.2% | 468.46 g·mol⁻¹ | C23H35Cl2N5O | 5 MG

NUCC-390 dihydrochloride is a small-molecule dihydrochloride salt that acts as a selective CXCR4 receptor agonist for research use. It induces CXCR4 internalization and has been reported to promote nerve recovery after neurodegeneration. The compound is supplied as a light yellow to yellow solid, with a molecular formula of C23H35Cl2N5O and a molecular weight of 468.46 g·mol⁻¹.

Selective CXCR4 receptor agonist that induces receptor internalization.
Reported to promote nerve recovery after neurodegeneration in vivo.
High purity suitable for research applications (98.2%).
Supplied as a solid; also available as a DMSO solution for convenience.
Stable when stored as recommended (powder at 4°C; in solvent -80°C or -20°C under nitrogen).

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4,009

Medchemexpress LLC HY-100453 5mg Medchemexpress, HO-3867 CAS:1172133-28-6 Purity:>98%

Medchemexpress, HY-100453 5mg HO-3867 CAS:1172133-28-6 HO-3867 is a selective and potent STAT3 inhibitor and shows good antitumor activity. 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.

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4,010

Medchemexpress LLC HY-101396 5mg Medchemexpress, ICA-069673 CAS:582323-16-8 Purity:>98%

Medchemexpress, HY-101396 5mg ICA-069673 CAS:582323-16-8 ICA-069673 is a KCNQ2/Q3 potassium channel activator with an IC 50 of 0.69 μM. 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.

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4,011

Medchemexpress LLC Frakefamide TFA | 00-00-0 | 99.2% | 677.64 g·mol⁻¹ | C32H35F4N5O7 | 5 MG

Frakefamide TFA is a peptide analgesic supplied as the trifluoroacetate salt that acts as a peripherally selective μ-opioid receptor agonist. It has limited ability to cross the blood-brain barrier, making it useful for research into peripheral analgesia and opioid receptor pharmacology. The product is provided in small solid quantities and as prepared DMSO solutions, with manufacturer-specified purity and molecular data.

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4,012

eMolecules 1820620-31-2 | 2-Amino-4-bromo-3-fluorobenzonitrile | Apollo Scientific | MFCD26407501 | 215.025 | C7H4BrFN2 | 95.000 | Nc1c(F)c(Br)ccc1C#N | 1g | 562428563

2-Amino-4-bromo-3-fluorobenzonitrile | Apollo Scientific | 1820620-31-2 | MFCD26407501 | 215.025 | C7H4BrFN2 | 95.000 | Nc1c(F)c(Br)ccc1C#N | 1g | 562428563

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4,013

Medchemexpress LLC 4-[[[[[2,6-dichloro-2'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]amino]carbonyl]amino]methyl]benzeneace | 2170477-75-3 | 98.1% | C23H17Cl2F3N2O4 | 10MG

RORγt inverse agonist 13 is a potent, orally active, and selective inverse agonist of the retinoic acid-related orphan receptor γt (RORγt), characterized for preclinical research use. The compound has been profiled for potency, purity, solubility, and storage stability to support in vitro and in vivo studies.

Potent RORγt inverse agonist with an IC50 of 63.8 nM.
Orally active and selective for RORγt.
High purity (~98.1%) suitable for research applications.
Supplied as a white to off-white solid for convenient handling.
Highly soluble in DMSO (100 mg/mL) for in vitro assays.
Formulation demonstrated ≥2.5 mg/mL in 10% DMSO/90% corn oil for in vivo dosing.
Stable as a powder at -20°C for long-term storage.
Intended for research use only; not for human therapeutic use.

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4,014

eMolecules 2073-35-0 | L-Iduronic acid | Apollo Scientific | MFCD00270009 | 194.139 | C6H10O7 | 98.000 | O[C@@H](C=O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O | 50mg | 562457427

L-Iduronic acid | Apollo Scientific | 2073-35-0 | MFCD00270009 | 194.139 | C6H10O7 | 98.000 | O[C@@H](C=O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O | 50mg | 562457427

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4,015

Medchemexpress LLC HY-106408 5mg Medchemexpress, Neu2000 CAS:640290-67-1 Purity:>98%

Medchemexpress, HY-106408 5mg Neu2000 CAS:640290-67-1 Neu2000 is an uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist. 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.

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4,016

Medchemexpress LLC N-(4-(4-(2-(diethylamino)-2-oxo-1-phenylethyl)piperazinyl)-3-fluorophenyl)-2-(3-pyridyl)benzamide | 1094873-14-9 | MFCD18782744 | 98.0% | C34H36FN5O2 | 10MG

JNJ-31020028 is a selective, brain-penetrant antagonist of the neuropeptide Y Y2 receptor used in neuroscience research. It demonstrates high potency in human and rodent Y2 assays and is supplied as a well-characterized, high-purity research compound with documented solubility and storage recommendations for powder and solution forms.

High purity suitable for research applications.
Brain-penetrant antagonist of neuropeptide Y Y2 receptor.
Demonstrated potency in human and rodent assays.
Compatible with common in vitro and in vivo formulations.
Documented solubility and storage conditions for reproducibility.

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4,017

Medchemexpress LLC Tolinapant | 1799328-86-1 | 99.81% | 539.68 | 1 ML

Tolinapant (ASTX660) is an orally bioavailable dual antagonist of cellular inhibitor of apoptosis protein (cIAP) and X-linked inhibitor of apoptosis protein (XIAP).

Orally bioavailable dual antagonist of cellular inhibitor of apoptosis protein (cIAP) and X-linked inhibitor of apoptosis protein (XIAP)
Being investigated in a single-agent Phase 1/2 clinical trial in patients with advanced solid tumors and lymphomas
Demonstrates antiproliferative activity against human MDA-MB-231 cells with an IC50 of 1.8 nM
Shows efficacy in HCC1806 xenografts in mice by causing moderate tumor growth inhibition
Available with a purity of 99.81%

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4,018

Apexbio Technology LLC Prasugrel 150322-43-3 100mg

Prasugrel (CAS 150322-43-3) is a small molecule inhibitor belonging to the thienopyridine chemical class that targets the P2Y12 subtype of adenosine diphosphate (ADP) receptors on platelets Through irreversible antagonism of these receptors prasugrel prevents ADP-mediated activation and aggregation of platelets This mode of action makes it a valuable tool for investigating platelet function thrombosis and the modulation of hemostatic pathways in preclinical and translational research models Prasugrel is frequently utilized in studies exploring the pharmacological regulation of platelet reactivity and ADP receptor signaling

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4,019

Medchemexpress LLC Urea, N-[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-N'-[3-[[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]amino]carbonyl... | 802555-85-7 | MFCD31666371 | 98.6% | 448.52 g/mol | C23H28N8O2 | 100MG

p32 Inhibitor M36 is a small-molecule inhibitor that binds directly to the mitochondrial protein p32 and inhibits its association with LyP-1. Supplied as a white to off-white solid for research use only, it is characterized by a molecular formula of C23H28N8O2, a molecular weight of approximately 448.5 g/mol, and high purity to support biochemical and cell-based studies.

Inhibits p32 and blocks p32-LyP-1 interaction.
Molecular formula C23H28N8O2.
Molecular weight 448.5 g/mol.
Purity 98.6% (LCMS).
Physical form solid, white to off-white powder.
Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (2 years) or -20°C (1 year).
Intended for research use only; not for human or clinical use.
Available in multiple pack sizes from 5 mg up to 500 mg.

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4,020

Cayman Chemical ANTIBODY UT-11 5mg

An mPGES-1 inhibitor; inhibits PGE2 production in both SK-N-AS human and BV-2 mouse cells (IC50s = 0.1 and 2 µM, respectively); reduces LPS-induced increases in a variety of cytokines, including CCL2, IL-6, and TNF-α, in the mouse hippocampus, but not kidney, without affecting the mRNA expression of Cox2 at 10 mg/kg, i.p.

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Fluorobenzenes

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Medchemexpress LLC Platicodigenin | 22327-82-8 | 520.70 | 5 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Nucc-390 dihydrochloride | 2749281-71-6 | MFCD32690075 | 98.2% | 468.46 g·mol⁻¹ | C23H35Cl2N5O | 5 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC HY-100453 5mg Medchemexpress, HO-3867 CAS:1172133-28-6 Purity:>98% Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC HY-101396 5mg Medchemexpress, ICA-069673 CAS:582323-16-8 Purity:>98% Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Frakefamide TFA | 00-00-0 | 99.2% | 677.64 g·mol⁻¹ | C32H35F4N5O7 | 5 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC 4-[[[[[2,6-dichloro-2'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]amino]carbonyl]amino]methyl]benzeneace | 2170477-75-3 | 98.1% | C23H17Cl2F3N2O4 | 10MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC HY-106408 5mg Medchemexpress, Neu2000 CAS:640290-67-1 Purity:>98% Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC N-(4-(4-(2-(diethylamino)-2-oxo-1-phenylethyl)piperazinyl)-3-fluorophenyl)-2-(3-pyridyl)benzamide | 1094873-14-9 | MFCD18782744 | 98.0% | C34H36FN5O2 | 10MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC Tolinapant | 1799328-86-1 | 99.81% | 539.68 | 1 ML Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More